@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA
> .
@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:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_head
{
this:
np:hasAssertion
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_assertion
;
np:hasProvenance
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_assertion
a
np:Assertion
.
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_provenance
a
np:Provenance
.
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0346153
a
ncit:C7057
.
dgn-gda:DGN7eb7afa00f1292720235a5217f759551
sio:SIO_000628
miriam-gene:675
,
lld:C0346153
;
a
sio:SIO_001121
.
}
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_provenance
{
dgn-np:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_assertion
dcterms:description
"[It is well established that rare mutations in BRCA2 predispose to familial breast cancer, but whether common variants at this locus contribute more modest risk to sporadic breast cancer has not been thoroughly investigated.]. 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:15317758
;
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:NP456502.RApz9gSbk3JMFlDzPGdAvthBnH0fCm_EqJhlP_lo8pNnA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:12+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" .
}