@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI
> .
@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:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_head
{
this:
np:hasAssertion
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_assertion
;
np:hasProvenance
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_assertion
a
np:Assertion
.
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_provenance
a
np:Provenance
.
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNedffafcba5667dd6f8b2190eac2e2a93
sio:SIO_000628
miriam-gene:7428
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_provenance
{
dgn-np:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_assertion
dcterms:description
"[Recent identification of VHL, c-met and TSC as candidate genes mutated in various types of renal carcinomas has greatly enhanced our understanding of the pathogenesis of renal carcinomas and has provided novel therapeutic options for patients with renal cancer.]. 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:11753085
;
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:NP500675.RAsxPbFT0g5AjHVJDO2ltPsoUCfziUSTWU43ycNbV2cFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}