@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0
> .
@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:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_head
{
this:
np:hasAssertion
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_assertion
;
np:hasProvenance
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_provenance
;
np:hasPublicationInfo
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_assertion
a
np:Assertion
.
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_provenance
a
np:Provenance
.
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_assertion
{
miriam-gene:7432
a
ncit:C16612
.
lld:C2973725
a
ncit:C7057
.
dgn-gda:DGN9229da08301de719d73a3bbdc11dc080
sio:SIO_000628
miriam-gene:7432
,
lld:C2973725
;
a
sio:SIO_001121
.
}
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_provenance
{
dgn-np:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_assertion
dcterms:description
"[To explore the underlying molecular mechanisms in this model, it was examined whether absence of the VIP gene might alter the expression of additional genes involved in the pathogenesis of PAH, as single-gene deletions, in the absence of hypoxia, rarely result in significant pulmonary vascular remodelling.]. 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:18166594
;
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:NP650384.RAf2WJ6YddSupvd7ZihxUt6alpX6ufVntR1UoYXGTtnf0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}