@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM
> .
@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 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:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_head
{
this:
np:hasAssertion
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion
;
np:hasProvenance
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance
;
np:hasPublicationInfo
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion
a
np:Assertion
.
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance
a
np:Provenance
.
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN4974e23083a58741f1cadb6a6d4982a7
sio:SIO_000628
miriam-gene:672
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance
{
dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion
dc:description
"[To establish whether or not inherited variation in BRCA1 influences prostate cancer risk we genotyped 1793 men with prostate cancer in Poland and 4570 controls for three founder mutations (C61G, 4153delA and 5382insC).]. 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:18090912
;
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:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}