@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0
> .
@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:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_head
{
this:
np:hasAssertion
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_assertion
;
np:hasProvenance
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_provenance
;
np:hasPublicationInfo
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_assertion
a
np:Assertion
.
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_provenance
a
np:Provenance
.
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_assertion
{
miriam-gene:23462
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNcf553b8bd1b585d42e2021d8816a4d89
sio:SIO_000628
miriam-gene:23462
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_provenance
{
dgn-np:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_assertion
dcterms:description
"[We previously reported that HEY1 and HEY2 selectively repress androgen receptor (AR) signaling in mammalian cell lines and have shown that in human tissue HEY1 is excluded from the nuclei in prostate cancer but not benign prostatic 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:21454491
;
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:NP187901.RAUo7SDlAtkjvcdD779u7vWYGfHYvlhdYOgt9AdKCx_H0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}