@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84
> .
@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:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_head
{
this:
np:hasAssertion
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_assertion
;
np:hasProvenance
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_provenance
;
np:hasPublicationInfo
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_assertion
a
np:Assertion
.
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_provenance
a
np:Provenance
.
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNbf7b84552c43be2019f41f0b35d10e6c
sio:SIO_000628
miriam-gene:675
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_provenance
{
dgn-np:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_assertion
dcterms:description
"[Women who have inherited a deleterious mutation in the BRCA1 or BRCA2 gene and those with the Lynch syndrome (hereditary nonpolyposis colorectal cancer) have the highest risk of developing ovarian cancer but account for only approximately 10% of those with the disease.]. 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:21521830
;
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:NP399260.RA1kZrTuCPyw8IryycxGOKl-PHijxjt0jHu_s8Dp2Pj84130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}