@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I
> .
@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:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_head
{
this:
np:hasAssertion
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_assertion
;
np:hasProvenance
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_assertion
a
np:Assertion
.
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_provenance
a
np:Provenance
.
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGNbb2c399c4f1fe7a776a1dcc1f9b8af93
sio:SIO_000628
miriam-gene:675
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_provenance
{
dgn-np:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_assertion
dcterms:description
"[To establish the contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer, we have analyzed both genes in DNA samples obtained from an affected individual in each of 112 families containing at least two cases of epithelial 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:10486320
;
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:NP213919.RAjfdWpDj0rjcsOLt01b2QLRLi5053y1dyaVT42h-nk3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:58+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" .
}