@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU
> .
@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:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_head
{
this:
np:hasAssertion
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_assertion
;
np:hasProvenance
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_provenance
;
np:hasPublicationInfo
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_assertion
a
np:Assertion
.
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_provenance
a
np:Provenance
.
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_assertion
{
miriam-gene:580
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGNe956b46d27f432ccdd73c8948d5d4f60
sio:SIO_000628
miriam-gene:580
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_provenance
{
dgn-np:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_assertion
dcterms:description
"[These results suggest that the contribution of the BARD1 germline variants to breast cancer predisposition is very limited, and that neither Cys557Ser nor Val507Met have an effect on familial breast cancer susceptibility.]. 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:16333312
;
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:NP482457.RABvhTWam6RAvtvGOQpG7te3A-F_2VSNpKV1pp-JEAvyU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}