@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo
> .
@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:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_head
{
this:
np:hasAssertion
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_assertion
;
np:hasProvenance
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_provenance
;
np:hasPublicationInfo
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_assertion
a
np:Assertion
.
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_provenance
a
np:Provenance
.
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_assertion
{
miriam-gene:6566
a
ncit:C16612
.
lld:C0020542
a
ncit:C7057
.
dgn-gda:DGN04b6059391396ec3b3f635fab61da03d
sio:SIO_000628
miriam-gene:6566
,
lld:C0020542
;
a
sio:SIO_001121
.
}
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_provenance
{
dgn-np:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_assertion
dcterms:description
"[Significant pulmonary hypertension developed 3 weeks after the administration of MCT, but gene therapy with CYP2J2 significantly attenuated the development of pulmonary hypertension and pulmonary vascular remodeling, without causing changes in systemic arterial pressure or heart rate.]. 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:20118222
;
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:NP308161.RARy-wt9WFNTRKMk2n88Do049JPUyn4qf5ZvX_sbiSllo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}