@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI
> .
@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:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_head
{
this:
np:hasAssertion
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion
;
np:hasProvenance
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion
a
np:Assertion
.
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance
a
np:Provenance
.
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN447a32f46d4c40ea54f32c0b05f2640c
sio:SIO_000628
miriam-gene:675
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance
{
dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion
dcterms:description
"[This preliminary finding does not support the assumption that the presence of BRCA1 and BRCA2 mutations in some infertility patients treated by fertility drugs could explain the subsequent development of epithelial ovarian cancer in these women.]. 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:10609497
;
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:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:01+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" .
}