@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw
> .
@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:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_head
{
this:
np:hasAssertion
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_assertion
;
np:hasProvenance
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_provenance
;
np:hasPublicationInfo
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_assertion
a
np:Assertion
.
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_provenance
a
np:Provenance
.
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_assertion
{
miriam-gene:5892
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN8fc2cb9e01942d0acdcfe384da6df5f7
sio:SIO_000628
miriam-gene:5892
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_provenance
{
dgn-np:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_assertion
dcterms:description
"[Mutations in RAD51D have been associated with an increased risk of hereditary ovarian cancer and although they have been observed in the context of breast and ovarian cancer families, the association with breast cancer is unclear.]. 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:23372765
;
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:NP389836.RA-TQv_d8Y56h44lzFLvZYZIj4XdkMWl-PtWPSSikR7pw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}