@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I
> .
@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:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_head
{
this:
np:hasAssertion
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_assertion
;
np:hasProvenance
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_assertion
a
np:Assertion
.
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_provenance
a
np:Provenance
.
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_assertion
{
miriam-gene:10606
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGNf3bb0cbc9faaa02e0ff161e7e1b801ae
sio:SIO_000628
miriam-gene:10606
,
lld:C0039585
;
a
sio:SIO_001121
.
}
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_provenance
{
dgn-np:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_assertion
dcterms:description
"[Establishing the functional consequences of androgen receptor mutations in vitro systems and correlating them with clinical presentation may ultimately provide an explanation for the variable clinical presentation of AIS and perhaps enable prediction of the response to androgen therapy in infants with PAIS.]. 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:8733002
;
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:NP687748.RATjw0AmMM-lUhzBXVu3iMOORRdtTjO2cDjpFC8M5Xd0I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}