@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA
> .
@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:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_head
{
this:
np:hasAssertion
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion
;
np:hasProvenance
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance
;
np:hasPublicationInfo
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion
a
np:Assertion
.
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance
a
np:Provenance
.
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNfde1f88f51eeca9ac5b638fa695386c4
sio:SIO_000628
miriam-gene:7428
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_provenance
{
dgn-np:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_assertion
dcterms:description
"[Even preneoplastic cystic structures may harbor entire loss of the chromosome 3, suggesting that loss of VHL gene function alone is not immediately causative for neoplastic growth, but further events, either mutations and deletions in other chromosomes or epigenetic or other than genetic phenomena, are required for tumor formation.]. 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:16261628
;
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:NP685656.RAvgF1DnHY9VujLu3ZVHtTTyW9N7Js6UT270OSMs7vhpA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}