@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I
> .
@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:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_head
{
this:
np:hasAssertion
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion
;
np:hasProvenance
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion
a
np:Assertion
.
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance
a
np:Provenance
.
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion
{
miriam-gene:1234
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN22e83dfcb9045dcc3e868124b449cc50
sio:SIO_000628
miriam-gene:1234
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_provenance
{
dgn-np:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_assertion
dcterms:description
"[Our data indicate that gene polymorphism of CCR2 V64I may influence the susceptibility and clinicopathological characteristics of prostate cancer and CCR5 Δ32 allele may also be an important risk factor for prostate cancer in Turkish men population.]. 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:22612293
;
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:NP324173.RABQtlFiDFLAkyl8-nxz4bq1zC3TZ6jAGRbGzxg-dlI0I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}