@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y
> .
@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:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_head
{
this:
np:hasAssertion
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_assertion
;
np:hasProvenance
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_assertion
a
np:Assertion
.
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_provenance
a
np:Provenance
.
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_assertion
{
miriam-gene:29072
a
ncit:C16612
.
lld:C0279702
a
ncit:C7057
.
dgn-gda:DGNb3cb9828b3b8dcb813ef9c5564777cb0
sio:SIO_000628
miriam-gene:29072
,
lld:C0279702
;
a
sio:SIO_001121
.
}
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_provenance
{
dgn-np:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_assertion
dcterms:description
"[Although von Hippel-Lindau (VHL) tumor suppressor gene alterations dominate the genetic landscape of clear cell renal cell carcinoma (ccRCC), recent studies have identified new ccRCC genes, including SETD2, KDM6A, KDM5C, BAP1 and PBRM1.]. 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:22949125
;
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:NP324711.RA4FfXBer71qbwP_fonNLzDUZLxc6jgIkSy8jzMUGiX6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}