@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y
> .
@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:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_head
{
this:
np:hasAssertion
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_assertion
;
np:hasProvenance
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_assertion
a
np:Assertion
.
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_provenance
a
np:Provenance
.
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1378703
a
ncit:C7057
.
dgn-gda:DGN8e4b8f4f83f51945a8d4d840e9a87349
sio:SIO_000628
miriam-gene:7248
,
lld:C1378703
;
a
sio:SIO_001121
.
}
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_provenance
{
dgn-np:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_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:NP344728.RAf5zxRPmcUSM_br8_8nhzEWOxKPtgwpH8fBamgBEFx-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}