@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_head
{
this:
np:hasAssertion
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_assertion
;
np:hasProvenance
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_provenance
;
np:hasPublicationInfo
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_assertion
a
np:Assertion
.
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_provenance
a
np:Provenance
.
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0001627
a
ncit:C7057
.
dgn-gda:DGNd9ecb16db8cbe0e29255d9409c68adb8
sio:SIO_000628
miriam-gene:367
,
lld:C0001627
;
a
sio:SIO_001121
.
}
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_provenance
{
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_assertion
dcterms:description
"[Recent developments in molecular biology have provided the opportunity to analyze the gene responsible for testicular determination, SRY, the androgen receptor gene and the gene encoding the cP450 enzyme specific for 21-hydroxylation, CYP21B, whose defects are responsible for congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:1306840
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP711835.RAJtet9w6ICuJsHAnCboibk_XCrYw0NwOHzWw1rMDb2Vk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}