This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.
The embedded RDF content will be recognized by any processor of HTML5 Microdata.
Namespace Prefixes
| Prefix | IRI |
|---|
| n7 | https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/ |
| n2 | http://purl.obolibrary.org/obo/ |
| wdrs | http://www.w3.org/2007/05/powder-s# |
| rdfs | http://www.w3.org/2000/01/rdf-schema# |
| obo | http://www.geneontology.org/formats/oboInOwl# |
| rdf | http://www.w3.org/1999/02/22-rdf-syntax-ns# |
| owl | http://www.w3.org/2002/07/owl# |
| xsdh | http://www.w3.org/2001/XMLSchema# |
Statements
- Subject Item
- n2:DOID_0111030
- rdf:type
-
owl:Class
- rdfs:subClassOf
-
_:vb50944080
n2:DOID_2352
- rdfs:label
-
hemochromatosis type 3
- wdrs:describedby
-
n7:doid.owl
- obo:id
-
DOID:0111030
- obo:hasDbXref
-
ORDO:225123
GARD:10093
OMIM:604250
UMLS_CUI:C1858664
SNOMEDCT_US_2021_09_01:719974003
MESH:C537248
- obo:hasExactSynonym
-
HFE3
hemochromatosis due to defect in transferrin receptor 2
TFR2-related hemochromatosis
- obo:hasOBONamespace
-
disease_ontology
- n2:IAO_0000115
-
A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.
- Subject Item
- _:vb50944080
- rdf:type
-
owl:Restriction
- owl:onProperty
-
n2:RO_0004019
- owl:someValuesFrom
-
n2:SO_0001537
- wdrs:describedby
-
n7:doid.owl