@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk
> .
@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:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_head
{
this:
np:hasAssertion
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_assertion
;
np:hasProvenance
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_assertion
a
np:Assertion
.
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_provenance
a
np:Provenance
.
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_assertion
{
miriam-gene:4359
a
ncit:C16612
.
lld:C0279702
a
ncit:C7057
.
dgn-gda:DGN1b1b5e9658de8665385bfbf05aa7f1cf
sio:SIO_000628
miriam-gene:4359
,
lld:C0279702
;
a
sio:SIO_001121
.
}
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_provenance
{
dgn-np:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_assertion
dcterms:description
"[The aim of this study was to evaluate the prevalence of chromosome 8q gain in clear cell renal cell carcinoma (CCRCC) and to correlate the findings with tumor phenotype and disease-specific survival (DSS).]. 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:22605478
;
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:NP781175.RA9jAl4EWTASaEWy3qNLhLq90-0CKdZz6Tf6VqYcOzfBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}