@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4
> .
@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:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_head
{
this:
np:hasAssertion
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_assertion
;
np:hasProvenance
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_provenance
;
np:hasPublicationInfo
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_assertion
a
np:Assertion
.
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_provenance
a
np:Provenance
.
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN37fd28cc75c998c9bd9a9bc3f1eaf5ea
sio:SIO_000628
miriam-gene:675
,
lld:C1333600
;
a
sio:SIO_001121
.
}
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_provenance
{
dgn-np:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_assertion
dcterms:description
"[Previous studies of mutations in BRCA1 or BRCA2 have used detection methods that may underestimate the actual frequency of mutations and have analyzed women using heterogeneous criteria for risk of hereditary 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:9667259
;
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:NP785752.RAq19D1FJZto86ewNbtor3230zimDuR9icnLaOvCeM8e4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}