@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw
> .
@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:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_head
{
this:
np:hasAssertion
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion
;
np:hasProvenance
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance
;
np:hasPublicationInfo
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion
a
np:Assertion
.
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance
a
np:Provenance
.
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion
{
miriam-gene:7528
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN8e285b379d564f3a32683616cd3f06f5
sio:SIO_000628
miriam-gene:7528
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_provenance
{
dgn-np:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_assertion
dcterms:description
"[In conclusion, we identified a new functional prostate cancer risk variant at the 8q24 locus, rs378854 allele G, that reduces binding of the YY1 protein and is associated with increased expression of PVT1 located 0.5 Mb downstream.]. 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:21814516
;
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:NP828273.RARgtd2eTVsMGe5-OPer3zqwd3S556TLHXDEtLuS9bHEw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}