@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8
> .
@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/v3.0.0/void/
> .
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_head
{
this:
np:hasAssertion
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion
;
np:hasProvenance
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance
;
np:hasPublicationInfo
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion
a
np:Assertion
.
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance
a
np:Provenance
.
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion
{
miriam-gene:7516
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNd7bd2179b735783ec37479c4bf0eabef
sio:SIO_000628
miriam-gene:7516
,
lld:C1140680
;
a
sio:SIO_001122
.
}
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_provenance
{
dgn-np:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_assertion
dcterms:description
"[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. 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:15734952
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP780477.RA4Uu5M8DliS4dpqJyOzmwmWmh83vbrzNfTw2uOX-O7c8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:32+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}