@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o
> .
@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:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_head
{
this:
np:hasAssertion
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion
;
np:hasProvenance
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion
a
np:Assertion
.
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance
a
np:Provenance
.
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C2931852
a
ncit:C7057
.
dgn-gda:DGN2acd0a1c5bd1e7244869a1105d0ac885
sio:SIO_000628
miriam-gene:7428
,
lld:C2931852
;
a
sio:SIO_001121
.
}
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_provenance
{
dgn-np:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_assertion
dcterms:description
"[Taken together, CAIX expression and VHL mutational status are able to stratify patients with clear cell RCC into distinct groups with regards to clinicopathological variables and prognosis, with low CAIX expression and absence of VHL mutation being associated with a poor clinicopathological phenotype and diminished survival.]. 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:18464292
;
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:NP773902.RAXulG_F8pWtpk0JyLp1AktBV7dUZ3w6EypbQ2DD61q0o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:28+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" .
}