@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw
> .
@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:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_head
{
this:
np:hasAssertion
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_assertion
;
np:hasProvenance
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_provenance
;
np:hasPublicationInfo
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_assertion
a
np:Assertion
.
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_provenance
a
np:Provenance
.
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGNc674025eef5b9ab8257a830fae6490f3
sio:SIO_000628
miriam-gene:7422
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_provenance
{
dgn-np:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_assertion
dcterms:description
"[Although the mechanism on the induction of VEGF gene is still unclear in human cancer tissue, we obtained the informative evidence indicating that p53 mutation is involved in VEGF expression of esophageal cancer.]. 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:10457902
;
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:NP725342.RAuKQUs7n57A5vnxH1vPF8W1oIxfNcMct20MOrrSWw5Vw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}