@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs
> .
@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:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_head
{
this:
np:hasAssertion
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_assertion
;
np:hasProvenance
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_provenance
;
np:hasPublicationInfo
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_assertion
a
np:Assertion
.
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_provenance
a
np:Provenance
.
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_assertion
{
miriam-gene:6047
a
ncit:C16612
.
lld:C0242787
a
ncit:C7057
.
dgn-gda:DGN24c7f4068847976997991e0b8a7f4f27
sio:SIO_000628
miriam-gene:6047
,
lld:C0242787
;
a
sio:SIO_001121
.
}
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_provenance
{
dgn-np:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_assertion
dcterms:description
"[Some AR ZFR point mutations observed in patients with partial androgen insensitivity syndrome or male breast cancer impair the interaction of AR with SNURF and also render AR refractory to the transcription-activating effect of SNURF.]. 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:10617653
;
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:NP804736.RA7Un_wT5YgFHcUumBzaNcJTxlXe0QpV3wIdjAX3Za2bs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+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" .
}