@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8
> .
@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:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_head
{
this:
np:hasAssertion
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_assertion
;
np:hasProvenance
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_provenance
;
np:hasPublicationInfo
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_assertion
a
np:Assertion
.
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_provenance
a
np:Provenance
.
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN79d4d337a8c982418ae0a732be85ced7
sio:SIO_000628
miriam-gene:672
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_provenance
{
dgn-np:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_assertion
dcterms:description
"[Considering these results, women who previously had BC and had survived ten years could be selected for BRCA1 analysis among family members at high risk of hereditary BC during genetic counselling.]. 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:20219108
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47772.RAA9Wdbg_IjLKe-CCxmJVOmUVZUyJNEuHolSy1Jx-A4X8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}