@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo
> .
@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:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_head
{
this:
np:hasAssertion
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_assertion
;
np:hasProvenance
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_provenance
;
np:hasPublicationInfo
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_assertion
a
np:Assertion
.
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_provenance
a
np:Provenance
.
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNbe80b1dde3c53debfd08e6679af16c42
sio:SIO_000628
miriam-gene:672
,
lld:C1140680
;
a
sio:SIO_001122
.
}
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_provenance
{
dgn-np:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_assertion
dcterms:description
"[This data indicates that the genetic burden of breast and ovarian cancer attributable to BRCA1 mutations in Lithuania is very high and supports the recommendation that all cases of breast and ovarian cancer in Lithuania be offered genetic testing.]. 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:20345474
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47782.RA8FU9G0_hZstewVZY7OuUVwDuBWzRG_wvIFyTWxczqUo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}