@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI
> .
@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:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_head
{
this:
np:hasAssertion
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_assertion
;
np:hasProvenance
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_provenance
;
np:hasPublicationInfo
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_assertion
a
np:Assertion
.
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_provenance
a
np:Provenance
.
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0001627
a
ncit:C7057
.
dgn-gda:DGNefa8589e8d240cd9091e1f90a587c91f
sio:SIO_000628
miriam-gene:367
,
lld:C0001627
;
a
sio:SIO_001121
.
}
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_provenance
{
dgn-np:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_assertion
dcterms:description
"[This ratio is greater in females than males from fetal life through adulthood, correlates with polymorphism in the androgen receptor gene in men, is feminine in XY androgen insensitivity syndrome, and masculinized in 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:20631003
;
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:NP264322.RAb0F795G0LsxFFm9B7n1utf8dMEq_EnhhMsUdju7aPHI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}