@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg
> .
@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:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_head
{
this:
np:hasAssertion
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_assertion
;
np:hasProvenance
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_provenance
;
np:hasPublicationInfo
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_assertion
a
np:Assertion
.
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_provenance
a
np:Provenance
.
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C0855197
a
ncit:C7057
.
dgn-gda:DGNec43a586475b6deca99538f7b342a973
sio:SIO_000628
miriam-gene:79017
,
lld:C0855197
;
a
sio:SIO_001121
.
}
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_provenance
{
dgn-np:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_assertion
dcterms:description
"[The risk of TC is markedly increased in subjects with androgen insensitivity and some authors have suggested that mutations in the androgen receptor (AR) gene or disorders of CAG and GGC repeats could be related to TC.]. 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:16172197
;
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:NP491158.RATVr-yDM2nyBj5cH-8XojV051UqsdOqYEKDRmSWHAePg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}