@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I
> .
@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:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_head
{
this:
np:hasAssertion
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_assertion
;
np:hasProvenance
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_provenance
;
np:hasPublicationInfo
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_assertion
a
np:Assertion
.
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_provenance
a
np:Provenance
.
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_assertion
{
miriam-gene:2274
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN9ae7b0c0aec2bfd7b17910730f414fcc
sio:SIO_000628
miriam-gene:2274
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_provenance
{
dgn-np:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_assertion
dcterms:description
"[These results offer general import beyond prostate cancer, given that nuclear FHL2 is characteristic of other human cancers where oncogenic transcription factors that drive disease are activated like the AR in prostate cancer.]. 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:23801747
;
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:NP485908.RAGZ3efBSmeTEI2acwl4U7escMlNplkGvzNlP-QdZUp5I130_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" .
}