@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4
> .
@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:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_head
{
this:
np:hasAssertion
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion
;
np:hasProvenance
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance
;
np:hasPublicationInfo
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion
a
np:Assertion
.
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance
a
np:Provenance
.
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion
{
miriam-gene:5376
a
ncit:C16612
.
lld:C0279702
a
ncit:C7057
.
dgn-gda:DGNed6020a66f088f57f1e6b42dd9e26bb0
sio:SIO_000628
miriam-gene:5376
,
lld:C0279702
;
a
sio:SIO_001121
.
}
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance
{
dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_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:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}