@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8
> .
@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:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_head
{
this:
np:hasAssertion
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_assertion
;
np:hasProvenance
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_assertion
a
np:Assertion
.
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_provenance
a
np:Provenance
.
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_assertion
{
miriam-gene:580
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN9d0747b467cc2c918d1a3c878850532f
sio:SIO_000628
miriam-gene:580
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_provenance
{
dgn-np:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_assertion
dcterms:description
"[Our findings suggest that BARD1 Cys557Ser is an ancient variant that confers risk of single and multiple primary breast cancers, and this risk extends to carriers of the BRCA2 999del5 mutation.]. 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:16768547
;
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:NP47898.RAOfa-XXveH49Uk3L5ykB_zFdnyv_rCbn3zGn3N-2dFG8130_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" .
}