@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8
> .
@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:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_head
{
this:
np:hasAssertion
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion
;
np:hasProvenance
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion
a
np:Assertion
.
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance
a
np:Provenance
.
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion
{
miriam-gene:6928
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNaffb43a37da9430bd7eda8874feb1c93
sio:SIO_000628
miriam-gene:6928
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance
{
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion
dcterms:description
"[We confirm recent reports that 8q24 variants identified to be associated with prostate cancer in men of European descent are also associated with prostate cancer in African Americans. Our report is the first to find evidence of association between SNPs near MSMB and prostate cancer in African Americans. Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been implicated to be independently associated, with respect to the widely reported SNP rs10993994 in the nearby gene MSMB, with prostate cancer in men of European descent.]. 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:20717903
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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" .
}