@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU
> .
@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/v3.0.0/void/
> .
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_head
{
this:
np:hasAssertion
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_assertion
;
np:hasProvenance
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_provenance
;
np:hasPublicationInfo
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_assertion
a
np:Assertion
.
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_provenance
a
np:Provenance
.
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGN1b366b9a1194eaa25a05bf6f98730ef3
sio:SIO_000628
miriam-gene:2944
,
lld:C0151744
;
a
sio:SIO_001121
.
}
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_provenance
{
dgn-np:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_assertion
dcterms:description
"[CNV in GSTM1 or GSTT1 or genotype combinations were not associated with an increased risk of IHD, myocardial infarction, ischemic cerebrovascular disease, ischemic stroke, or any ischemic vascular event in studies individually or combined or in the meta-analyses.]. 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:21562205
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP438044.RAqfhQtDW219rUVTZ-NKVlAiXQH9Lv-6C8AAYkjcuHAtU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:55+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}