@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw
> .
@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:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_head
{
this:
np:hasAssertion
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_assertion
;
np:hasProvenance
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_provenance
;
np:hasPublicationInfo
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_assertion
a
np:Assertion
.
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_provenance
a
np:Provenance
.
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_assertion
{
miriam-gene:4514
a
ncit:C16612
.
lld:C0009375
a
ncit:C7057
.
dgn-gda:DGN1a7cf472cad21983fd0eb5d2bfed3b65
sio:SIO_000628
miriam-gene:4514
,
lld:C0009375
;
a
sio:SIO_001121
.
}
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_provenance
{
dgn-np:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_assertion
dcterms:description
"[We have shown that expression levels of COXIII, a mitochondrial gene encoding one of the 13 subunits of cytochrome c oxidase, are abnormally low in colon tumors and colonic tissue at genetic risk for developing tumors but increase following in vitro treatment of HT29 human colonic adenocarcinoma cells with the fatty acid butyrate.]. 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:1655774
;
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:NP495512.RAgMdM_4RVw0r6NTFVS5LuGM5ntKqr5TQD06ovCPWbHuw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}