@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78
> .
@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:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_head
{
this:
np:hasAssertion
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_assertion
;
np:hasProvenance
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_provenance
;
np:hasPublicationInfo
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_assertion
a
np:Assertion
.
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_provenance
a
np:Provenance
.
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0740457
a
ncit:C7057
.
dgn-gda:DGN4abf01f72462066f83ab7fd832951062
sio:SIO_000628
miriam-gene:7248
,
lld:C0740457
;
a
sio:SIO_001121
.
}
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_provenance
{
dgn-np:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_assertion
dcterms:description
"[Clear cell renal cell carcinoma (ccRCC) is the most common histological subtype of kidney cancer and is often characterized by mutations or deletions of the Von Hippel Lindau (VHL) tumour suppressor gene.]. 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:23785518
;
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:NP247215.RABK3loWhlKCW6MPg2z7DM1bg2iA6U4LnzS285VIxL_78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}