@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s
> .
@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:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_head
{
this:
np:hasAssertion
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_assertion
;
np:hasProvenance
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_provenance
;
np:hasPublicationInfo
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_assertion
a
np:Assertion
.
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_provenance
a
np:Provenance
.
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN58a89abda1434272381f5bac70d251e2
sio:SIO_000628
miriam-gene:2952
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_provenance
{
dgn-np:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_assertion
dcterms:description
"[The GSTA1*-69T and GSTO2*D142 variants are associated with the significant increased risk of asthma development in our study population, while GSTM1, GSTP1 and GSTT1 genotype distributions were nearly equal between the control group and asthmatics.]. 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:22040239
;
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:NP179594.RAECxOWzTwIbOg3HNJz0TqcEADnkVXgmyuwrCkGkUt93s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}