@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4
> .
@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:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_head
{
this:
np:hasAssertion
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion
;
np:hasProvenance
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance
;
np:hasPublicationInfo
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion
a
np:Assertion
.
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance
a
np:Provenance
.
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN63e54b0499ad9dc1146c3726d1fbfbb5
sio:SIO_000628
miriam-gene:672
,
lld:C1333600
;
a
sio:SIO_001121
.
}
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_provenance
{
dgn-np:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_assertion
dcterms:description
"[To estimate the proportion of ovarian cancers attributable to founding mutations in BRCA1 and BRCA2 in the Jewish population and the familial cancer risks associated with each, we interviewed 213 Jewish women with ovarian cancer at 11 medical centers in North America and Israel and offered these women genetic testing for the three founder mutations.]. 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:10739756
;
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:NP228089.RAUgfApp6_CYlW2OJ32tGnU_-hcwsKevng0H5iy2eC8z4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}