@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc
> .
@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:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_head
{
this:
np:hasAssertion
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_assertion
;
np:hasProvenance
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_provenance
;
np:hasPublicationInfo
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_assertion
a
np:Assertion
.
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_provenance
a
np:Provenance
.
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_assertion
{
miriam-gene:6045
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGNeba6d29738c92b4e887d3ebf6d5e8132
sio:SIO_000628
miriam-gene:6045
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_provenance
{
dgn-np:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_assertion
dcterms:description
"[Although von Hippel-Lindau (VHL) tumor suppressor gene alterations dominate the genetic landscape of clear cell renal cell carcinoma (ccRCC), recent studies have identified new ccRCC genes, including SETD2, KDM6A, KDM5C, BAP1 and PBRM1.]. 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:22949125
;
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:NP816967.RAk1hm_QU4rdBuJ7XleAMmgF7Mx-uvp2_Wz051Sg9yEoc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}