@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E
> .
@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:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_head
{
this:
np:hasAssertion
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_assertion
;
np:hasProvenance
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_provenance
;
np:hasPublicationInfo
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_assertion
a
np:Assertion
.
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_provenance
a
np:Provenance
.
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_assertion
{
miriam-gene:4214
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNcea70e293ea61b8dba76c787ca0ed6c3
sio:SIO_000628
miriam-gene:4214
,
lld:C0678222
;
a
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.
}
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_provenance
{
dgn-np:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_assertion
dcterms:description
"[In a previous study, we demonstrated that the minor alleles at three of these SNPs, in FGFR2, TNRC9 and MAP3K1, also confer increased risks of breast cancer for BRCA1 or BRCA2 mutation carriers.]. 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:19656774
;
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:NP260647.RAU6beJwstbtGYox6_OSzrZPU39pcTq7ErfcaJMgP1X1E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}