@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY
> .
@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:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_head
{
this:
np:hasAssertion
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_assertion
;
np:hasProvenance
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_provenance
;
np:hasPublicationInfo
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_assertion
a
np:Assertion
.
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_provenance
a
np:Provenance
.
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_assertion
{
miriam-gene:1475
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN606f6586eb9f2bbdb8810df58e5cce91
sio:SIO_000628
miriam-gene:1475
,
lld:C0024117
;
a
sio:SIO_001121
.
}
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_provenance
{
dgn-np:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_assertion
dcterms:description
"[Here we report that genetic variation, smoking, and COPD can all elevate levels of CSTA expression in lung small airway epithelia, with still further upregulation in squamous cell carcinoma (SCC), an NSCLC subtype.]. 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:21325429
;
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:NP443449.RAKgKs_7NUCbJSPcwoIXQy2WqHWNCSuK5obMbKrw1CbQY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}