@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg
> .
@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:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_head
{
this:
np:hasAssertion
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_assertion
;
np:hasProvenance
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_provenance
;
np:hasPublicationInfo
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_assertion
a
np:Assertion
.
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_provenance
a
np:Provenance
.
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_assertion
{
miriam-gene:6794
a
ncit:C16612
.
lld:C2314896
a
ncit:C7057
.
dgn-gda:DGNa96ef63c00f5f66824f4b8e538dbb1e5
sio:SIO_000628
miriam-gene:6794
,
lld:C2314896
;
a
sio:SIO_001121
.
}
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_provenance
{
dgn-np:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_assertion
dcterms:description
"[Germline mutations in BRCA2 have been shown to predispose to both breast and pancreatic cancer, germline mutations in p16 to melanoma and pancreatic cancer (the FAMMM syndrome), and genetic mutations in STK11/LKB1 to pancreatic cancer in patients with the Peutz-Jeghers Syndrome (PJS).]. 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:10436789
;
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:NP764640.RAtYRmhlvd_1PXoSwzbSTc4GcEPnqRShxDy0oQGla2efg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}