@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8
> .
@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:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_head
{
this:
np:hasAssertion
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion
;
np:hasProvenance
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion
a
np:Assertion
.
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance
a
np:Provenance
.
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN250870d2c5d5029642a9a3951a42b200
sio:SIO_000628
miriam-gene:2272
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_provenance
{
dgn-np:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_assertion
dcterms:description
"[Here we show that the von Hippel-Lindau (VHL) tumour suppressor protein, pVHL, which is inactivated in hereditary and sporadic forms of renal cell carcinoma, localizes to the mitotic spindle in mammalian cells and its functional inactivation provokes spindle misorientation, spindle checkpoint weakening and chromosomal instability.]. 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:19620968
;
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:NP227536.RAFiVMAjLXSX9uxRY0hFMPYJrJhCOPpTO1Kb-1vz0nr-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}