@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q
> .
@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:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_head
{
this:
np:hasAssertion
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_assertion
;
np:hasProvenance
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_assertion
a
np:Assertion
.
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_provenance
a
np:Provenance
.
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_assertion
{
miriam-gene:4582
a
ncit:C16612
.
lld:C0152171
a
ncit:C7057
.
dgn-gda:DGN430803716159e18c97869798924939c9
sio:SIO_000628
miriam-gene:4582
,
lld:C0152171
;
a
sio:SIO_001121
.
}
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_provenance
{
dgn-np:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_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:NP675577.RADcSHHpbLTxP5v_z6DnYF0cQ_eTMsFE6aRzi1_mCQS3Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}