@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08
> .
@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:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_head
{
this:
np:hasAssertion
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion
;
np:hasProvenance
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance
;
np:hasPublicationInfo
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion
a
np:Assertion
.
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance
a
np:Provenance
.
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion
{
miriam-gene:3091
a
ncit:C16612
.
lld:C0740457
a
ncit:C7057
.
dgn-gda:DGN74c1a6e762ce221a3d3f2a2e0551fff4
sio:SIO_000628
miriam-gene:3091
,
lld:C0740457
;
a
sio:SIO_001121
.
}
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance
{
dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion
dcterms:description
"[Clear cell renal cell carcinoma (ccRCC) is the most common form of kidney cancer and is often linked to loss of chromosome 3p, which harbors the VHL tumor suppressor gene, loss of chromosome 14q, which includes HIF1A, and gain of chromosome 5q.]. 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:24332042
;
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:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}