@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg
> .
@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:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_head
{
this:
np:hasAssertion
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_assertion
;
np:hasProvenance
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_assertion
a
np:Assertion
.
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_provenance
a
np:Provenance
.
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C0034067
a
ncit:C7057
.
dgn-gda:DGNa108e6b84c053e9abb008d17face3eb8
sio:SIO_000628
miriam-gene:2052
,
lld:C0034067
;
a
sio:SIO_001121
.
}
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_provenance
{
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_assertion
dcterms: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_curated
;
sio:SIO_000772
miriam-pubmed:9288046
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP14845.RAqtOLla-TRzFKay6nMWipb0qTHZCgALSrcFB_iBtzAhg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:05+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" .
}