@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM
> .
@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:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_head
{
this:
np:hasAssertion
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_assertion
;
np:hasProvenance
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_provenance
;
np:hasPublicationInfo
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_assertion
a
np:Assertion
.
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_provenance
a
np:Provenance
.
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C1334978
a
ncit:C7057
.
dgn-gda:DGNc1587a0b0f4a126978ede9fcb0a1e754
sio:SIO_000628
miriam-gene:7428
,
lld:C1334978
;
a
sio:SIO_001121
.
}
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_provenance
{
dgn-np:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_assertion
dcterms:description
"[Loss of von Hippel-Lindau tumor suppressor gene function occurs in familial and most sporadic clear cell renal cell carcinoma, resulting in the aberrant expression of genes that control cell proliferation, metabolism, invasion and angiogenesis.]. 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:18950731
;
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:NP376004.RAh5t0i6JrO8TkevNenaGYdjDMB1FwZGJ_WGbFuRAvLsM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}