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http://rdf.disgenet.org/nanopublications.trig#NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_head
{
this:
np:hasAssertion
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion
;
np:hasProvenance
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion
a
np:Assertion
.
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance
a
np:Provenance
.
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNfa0e86792b30ceec7b713ffd68231f31
sio:SIO_000628
miriam-gene:1029
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance
{
dgn-np:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion
dcterms:description
"[Our findings show that few patients with BC and CMM who lacked family histories of these cancers are carriers of deleterious germline mutations in four of the five genes we examined.]. 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:17624602
;
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:NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
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"v2.1.0" .
}