@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE
> .
@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:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_head
{
this:
np:hasAssertion
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_assertion
;
np:hasProvenance
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_provenance
;
np:hasPublicationInfo
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_assertion
a
np:Assertion
.
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_provenance
a
np:Provenance
.
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_assertion
{
miriam-gene:5462
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN0b827323e5e621a31e410467cb5dd691
sio:SIO_000628
miriam-gene:5462
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_provenance
{
dgn-np:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_assertion
dcterms:description
"[Although this study does not directly confirm associations of the three specific SNPs (cited above), it corroborates reported signals of association in 8q24 reaffirming that genetic variation on 8q24 influences susceptibility to PC in men of European ance]. 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:19562729
;
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:NP68079.RA4JTUe_xacEpgtKJz2Yc7pN8RRWOQ7LL9hQDevblZLyE130_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" .
}