@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_head
{
this:
np:hasAssertion
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_assertion
;
np:hasProvenance
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_assertion
a
np:Assertion
.
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_provenance
a
np:Provenance
.
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_assertion
{
miriam-gene:9223
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGNe329188359c69f7a48f1d8428300928f
sio:SIO_000628
miriam-gene:9223
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_provenance
{
dgn-np:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_assertion
dcterms:description
"[In addition, a review of BAP1 cancer syndrome families reported to date indicates that the location of the BAP1 mutation does not have any bearing on the spectrum of cancer types observed, either for mesothelial or melanocytic tumors.]. 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:23849051
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP818189.RAi0gOcGpSuzYj6GrwJjgfp7EXWaHn61GU0BVMP-MNnj8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:56+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}