@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA
> .
@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:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_head
{
this:
np:hasAssertion
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_assertion
;
np:hasProvenance
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_provenance
;
np:hasPublicationInfo
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_assertion
a
np:Assertion
.
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_provenance
a
np:Provenance
.
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN7677750f533d707e9d5cd4e50e7aa01c
sio:SIO_000628
miriam-gene:675
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_provenance
{
dgn-np:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_assertion
dcterms:description
"[In addition, 5 BRCA2-related breast cancers and 66 breast cancers of untested patients at intermediate risk and 19 breast cancers of untested patients at high risk of hereditary disease on the basis of family history were evaluated.]. 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:16603649
;
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:NP679347.RAfTBq8XqKQgUjeHqoZ0IdBj5m8aXeP8u90k8XHTgXylA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}