@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM
> .
@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:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_head
{
this:
np:hasAssertion
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_assertion
;
np:hasProvenance
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_provenance
;
np:hasPublicationInfo
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_assertion
a
np:Assertion
.
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_provenance
a
np:Provenance
.
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN3852aa3993036b2b4a1596165ae58237
sio:SIO_000628
miriam-gene:4524
,
lld:C0149721
;
a
sio:SIO_001122
.
}
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_provenance
{
dgn-np:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_assertion
dcterms:description
"[This study was designed to investigate, in the Turkish population, the association of methylene tetrahydrofolate reductase (MTHFR) C677T polymorphism and left ventricular hypertrophy (LVH) in patients with type II diabetes mellitus.]. 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:15469701
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP141021.RA9GOO4y7BVn2VZj5VByWD1ulIJSNi11GwNmERvQ0bPHM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:13+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: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" .
}