@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA
> .
@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:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_head
{
this:
np:hasAssertion
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_assertion
;
np:hasProvenance
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_provenance
;
np:hasPublicationInfo
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_assertion
a
np:Assertion
.
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_provenance
a
np:Provenance
.
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN7358c48ee40c0e9922a118ea934b8405
sio:SIO_000628
miriam-gene:675
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_provenance
{
dgn-np:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_assertion
dcterms:description
"[These results suggest that both genetic and nongenetic factors modify cancer risks among BRCA1 and BRCA2 mutation carriers, and that genetic modifiers and other familial factors may influence risk specifically for either breast or ovarian cancer.]. 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:16537453
;
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:NP156704.RAn-A42CQiWiMh1gLh9v7oJ-wH25jS4zEE2fbQN1SAlHA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}