@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c
> .
@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:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_head
{
this:
np:hasAssertion
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_assertion
;
np:hasProvenance
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_assertion
a
np:Assertion
.
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_provenance
a
np:Provenance
.
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGNe8a5b9232b954dd1641a1a70b6cd4083
sio:SIO_000628
miriam-gene:2056
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_provenance
{
dgn-np:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_assertion
dcterms:description
"[Dysfunction of the VHL protein causes accumulation and activation of hypoxia inducible factor (HIF) which can be demonstrated in earliest stages of tumorigenesis and is followed by expression of VEGF, erythropoietin, nitric oxide synthase and glucose transporter 1 in VHL-deficient tumor cells.]. 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:23400300
;
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:NP681069.RAnWnZUXDaYNWCTlB35U0koyAeFHHj1_EFVHu9f-4GL-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:51+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" .
}