@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_head
{
this:
np:hasAssertion
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_assertion
;
np:hasProvenance
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_provenance
;
np:hasPublicationInfo
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_assertion
a
np:Assertion
.
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_provenance
a
np:Provenance
.
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNf39254898dc95a429c42c04a87333ae7
sio:SIO_000628
miriam-gene:675
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_provenance
{
dgn-np:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_assertion
dcterms:description
"[To explore the way in which asymptomatic women diagnosed with mutation in BRCA1 or BRCA2 genes give meaning to their family scripts and to the dialectic between being concurrently healthy and at high risk for breast and ovarian cancer, vis-a-vis their way of coping with risks.]. 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:19753503
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP763134.RACCRApuGBTB6OV2vwq1NKVnZF3Xb15gIVkTBDtTHaERM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}