@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A
> .
@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:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_head
{
this:
np:hasAssertion
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_assertion
;
np:hasProvenance
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_provenance
;
np:hasPublicationInfo
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_assertion
a
np:Assertion
.
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_provenance
a
np:Provenance
.
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_assertion
{
miriam-gene:1589
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGN1336a9b44bbb00f160a6a276834015a9
sio:SIO_000628
miriam-gene:1589
,
lld:C0206081
;
a
sio:SIO_001121
.
}
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_provenance
{
dgn-np:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_assertion
dcterms:description
"[Heterozygosity for CYP21A2 mutations in females increases their risk of clinically manifesting hyperandrogenism and the present study was designed to seek evidence on the prevalence and consequences of heterozygous CYP21A2 mutations in children with premature adrenarche and adolescents with hyperandrogenemia.]. 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:23045419
;
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:NP485770.RAY2T1ZBEEhOQvIOrx51jWQSK5cJFiBZNihPL0T-8DY3A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}