@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_head
{
this:
np:hasAssertion
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_assertion
;
np:hasProvenance
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_provenance
;
np:hasPublicationInfo
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_assertion
a
np:Assertion
.
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_provenance
a
np:Provenance
.
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN0566ede7658ce656f1727936f7119f76
sio:SIO_000628
miriam-gene:7428
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_provenance
{
dgn-np:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_assertion
dcterms:description
"[These mutations may cause substitutions of specific amino acid residue and functional change of VHL protein (pVHL), which leads to the oncogenesis of the particular tumor types that characterize the different VHL disease types.]. 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:15870918
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP493196.RAYsF8oAd5fww6nOC9nSvfNr8e4_xW6k3vXc3rL2CbHpM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:28+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}