@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE
> .
@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:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_head
{
this:
np:hasAssertion
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion
;
np:hasProvenance
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance
;
np:hasPublicationInfo
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion
a
np:Assertion
.
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance
a
np:Provenance
.
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_assertion
{
miriam-gene:768
a
ncit:C16612
.
lld:C2931852
a
ncit:C7057
.
dgn-gda:DGN2ba1d3c6c8ed53f1c1a899bde7ebeba1
sio:SIO_000628
miriam-gene:768
,
lld:C2931852
;
a
sio:SIO_001121
.
}
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_provenance
{
dgn-np:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_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-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:NP571333.RAp-uobzOEvYHpA9_UoaZ_jx6d69l7ySY79zfw67tg0OE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}