@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_head
{
this:
np:hasAssertion
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_assertion
;
np:hasProvenance
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_assertion
a
np:Assertion
.
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_provenance
a
np:Provenance
.
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_assertion
{
miriam-gene:847
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN8d922a8599a9af874d6f7314deec06e0
sio:SIO_000628
miriam-gene:847
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_provenance
{
dgn-np:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_assertion
dcterms:description
"[This is the first study to implicate genetic variation in catalase in susceptibility to EHYT and suggests that polymorphisms in promoter regions may be particularly relevant to the study of complex diseases.]. 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:11479740
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP325597.RAuDKVURCKffglD8f0hx-l5pLZVTuB_wOomUomsq4azXw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:13+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}