@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8
> .
@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:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_head
{
this:
np:hasAssertion
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_assertion
;
np:hasProvenance
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_assertion
a
np:Assertion
.
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_provenance
a
np:Provenance
.
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_assertion
{
miriam-gene:10063
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNe5c764f0817c0502c6a4baee4bcca619
sio:SIO_000628
miriam-gene:10063
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_provenance
{
dgn-np:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_assertion
dcterms:description
"[Because our data imply that up-regulation of COX17 function and increased CCO activity are frequent features of lung carcinogenesis, we suggest that selective suppression of components of the CCO complex might hold promise for development of a new strategy for treating lung cancers.]. 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:14612491
;
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:NP755255.RArrAd01pEhLRVFEoZqTKs6x2VIpNN_4fX8WTfL7ikM-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}