@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ
> .
@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 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:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_head
{
this:
np:hasAssertion
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_assertion
;
np:hasProvenance
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_assertion
a
np:Assertion
.
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_provenance
a
np:Provenance
.
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGNf87b45d3e0dd8992702f864178abd1a7
sio:SIO_000628
miriam-gene:2052
,
lld:C0024117
;
a
sio:SIO_001122
.
}
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_provenance
{
dgn-np:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_assertion
dct:description
"[We investigated whether polymorphisms in the gene for microsomal epoxide hydrolase (mEPHX), an enzyme involved in this protective process, had any bearing on individual susceptibility to the development of chronic obstructive pulmonary disease (COPD) and emphysema.]. 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:9288046
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP45061.RAgcNteM5YnryDL_2bmx8_omfMVIAOVxfz5NO09E7y1CQ130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}