Q1031536: Difference between revisions

@@ label / nl / label / nl @@
-Campomele dysplasie
+campomele dysplasie
@@ label / tr / label / tr @@
+Kampomelik displazi
@@ label / bs / label / bs @@
+Kampomelna displazija
@@ label / sr / label / sr @@
+Кампомелични синдром
@@ description / uk / description / uk @@
+хвороба
@@ Property / Disease Ontology ID: DOID:0050463 / reference @@
+stated in: Disease Ontology
retrieved: 30 November 2020Timestamp +2020-11-30T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2020-11-30T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Disease Ontology ID: DOID:0050463 / reference @@
-stated in: Disease Ontology
retrieved: 28 August 2019Timestamp +2019-08-28T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2019-08-28T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / subclass of: osteochondrodysplasia / reference @@
+stated in: Disease Ontology
retrieved: 30 November 2020Timestamp +2020-11-30T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2020-11-30T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / subclass of: osteochondrodysplasia / reference @@
-stated in: Disease Ontology
retrieved: 15 May 2019Timestamp +2019-05-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2019-05-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / subclass of: autosomal dominant disease / reference @@
+stated in: Disease Ontology
retrieved: 30 November 2020Timestamp +2020-11-30T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2020-11-30T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / subclass of: autosomal dominant disease / reference @@
-stated in: Disease Ontology
retrieved: 15 May 2019Timestamp +2019-05-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2019-05-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / exact match: http://purl.obolibrary.org/obo/DOID_0050463 / reference @@
+stated in: Disease Ontology
retrieved: 30 November 2020Timestamp +2020-11-30T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2020-11-30T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / exact match: http://purl.obolibrary.org/obo/DOID_0050463 / reference @@
-stated in: Disease Ontology
retrieved: 28 August 2019Timestamp +2019-08-28T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2019-08-28T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / exact match: http://identifiers.org/doid/DOID:0050463 / reference @@
+stated in: Identifiers.org
reference URL: https://registry.identifiers.org/registry/doid
@@ Property / exact match: http://identifiers.org/doid/DOID:0050463 / reference @@
-stated in: Identifiers.org
reference URL: http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
@@ Property / instance of @@
-disease
@@ Property / instance of: disease / rank @@
-Normal rank
@@ Property / instance of: disease / reference @@
-stated in: Disease Ontology
retrieved: 15 May 2019Timestamp +2019-05-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
Disease Ontology ID: DOID:0050463
-Timestamp
++2019-05-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / instance of: disease / reference @@
-stated in: Prenatal bowing and thickening of tubular bones, with multiple cutaneous dimples in arms and legs; a congenital syndrome of mechanical origin.
@@ Property / instance of @@
+class of disease
@@ Property / instance of: class of disease / rank @@
+Normal rank
@@ Property / KEGG ID @@
+H00442
@@ Property / KEGG ID: H00442 / rank @@
+Normal rank
@@ Property / Genetics Home Reference Conditions ID @@
+campomelic-dysplasia
@@ Property / Genetics Home Reference Conditions ID: campomelic-dysplasia / rank @@
+Normal rank
@@ Property / image @@
+Kyphoscoliosis hereditary sensory autonomic neuropathy III.jpg
+Normal rank
@@ Property / UniProt disease ID @@
+DI-01311
@@ Property / UniProt disease ID: DI-01311 / rank @@
+Normal rank
@@ Property / WikiProjectMed ID @@
+Campomelic dysplasia
@@ Property / WikiProjectMed ID: Campomelic dysplasia / rank @@
+Normal rank
@@ Property / Mondo ID @@
+MONDO_0007251
@@ Property / Mondo ID: MONDO_0007251 / rank @@
+Normal rank
@@ Property / Miraheze article ID @@
+lgbta:Campomelic_Dysplasia
@@ Property / Miraheze article ID: lgbta:Campomelic_Dysplasia / rank @@
+Normal rank
@@ links / trwiki / name / links / trwiki / name @@
+Kampomelik displazi
@@ links / bswiki / name / links / bswiki / name @@
+Kampomelna displazija
@@ links / srwiki / name / links / srwiki / name @@
+Кампомелични синдром