@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc
> .
@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:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_head
{
this:
np:hasAssertion
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_assertion
;
np:hasProvenance
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_assertion
a
np:Assertion
.
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_provenance
a
np:Provenance
.
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_assertion
{
miriam-gene:4582
a
ncit:C16612
.
lld:C2973725
a
ncit:C7057
.
dgn-gda:DGN60b8b10c86ef3d7d7bb103a2584c6a57
sio:SIO_000628
miriam-gene:4582
,
lld:C2973725
;
a
sio:SIO_001121
.
}
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_provenance
{
dgn-np:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_assertion
dcterms:description
"[The lack of MCD results in an inhibition of fatty acid oxidation, which in turn promotes glucose oxidation and prevents the shift in metabolism toward glycolysis in the vascular media, which drives the development of pulmonary arterial hypertension in wild-type mice.]. 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:20702857
;
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:NP274816.RAcSTsNsrmmMVBHrVxRcsDoIwHy1xPXHD6CpqlxBn-qVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}