@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0
> .
@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:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_head
{
this:
np:hasAssertion
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_assertion
;
np:hasProvenance
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_assertion
a
np:Assertion
.
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_provenance
a
np:Provenance
.
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0266539
a
ncit:C7057
.
dgn-gda:DGN887c68ba130e4bd0c61190034964c52a
sio:SIO_000628
miriam-gene:7428
,
lld:C0266539
;
a
sio:SIO_001121
.
}
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_provenance
{
dgn-np:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_assertion
dcterms:description
"[We conclude that the selection pressure to mutate VHL exon II during tumorigenesis does not relate to loss of CCT binding but may reflect quantitative or qualitative defects in HIF binding and/or in pVHL-dependent ubiquitin ligase activity.]. 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:11865071
;
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:NP579705.RAUs1AG26XDKSIjgCcRrzMlmDZs5VpyDtQ7BuFWjkKv-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}