@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s
> .
@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:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_head
{
this:
np:hasAssertion
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_assertion
;
np:hasProvenance
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_provenance
;
np:hasPublicationInfo
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_assertion
a
np:Assertion
.
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_provenance
a
np:Provenance
.
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_assertion
{
miriam-gene:843
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN3b8116c931e03d23c31d2ec29160a4b9
sio:SIO_000628
miriam-gene:843
,
lld:C1140680
;
a
sio:SIO_001122
.
}
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_provenance
{
dgn-np:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_assertion
dcterms:description
"[To evaluate whether the CASP8 D302H (CASP10 V410I) polymorphisms modify breast or ovarian cancer risk in BRCA1 and BRCA2 mutation carriers, we analyzed 7,353 (7,227) subjects of white European origin provided by 19 (18) study groups that participate in the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).]. 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:20978178
;
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:NP90995.RAtV-zn2JZaIHeM0KseHwOkeX9qsgghiMKXrqPF40r25s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}