@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo
> .
@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/v4.0.0/void/
> .
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_head
{
this:
np:hasAssertion
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_assertion
;
np:hasProvenance
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_assertion
a
np:Assertion
.
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_provenance
a
np:Provenance
.
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGNb8a95ae50018592aa22b5aaea2343d95
sio:SIO_000628
miriam-gene:7428
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_provenance
{
dgn-np:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_assertion
dcterms:description
"[In the past decade, our understanding of the genetic mutations associated with sporadic forms of RCC has increased considerably, with the most common mutations in clear cell RCC seen in the VHL, PBRM1, BAP1, and SETD2 genes.]. 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:25365943
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1234526.RA2cIL0KRAfd6BUx8vhOgaePGvqc0kf3Ybqpmo7O91Ayo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:05+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}