@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4
> .
@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:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_head
{
this:
np:hasAssertion
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_assertion
;
np:hasProvenance
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_provenance
;
np:hasPublicationInfo
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_assertion
a
np:Assertion
.
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_provenance
a
np:Provenance
.
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_assertion
{
miriam-gene:4569
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNc158e6e81981f9e03ee697c6a6d19388
sio:SIO_000628
miriam-gene:4569
,
lld:C0149721
;
a
sio:SIO_001122
.
}
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_provenance
{
dgn-np:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_assertion
dcterms:description
"[The noncoding mitochondrial sequence alteration (A4401G) at the junction of tRNA (Met) and tRNA (Gln) alters mitochondrial function, implicating this mutation in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives.]. 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:18701880
;
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:NP141031.RA2aIUYd4MZjguB6pSXeIsuekpjdOkNN2Rg4xhTVctdi4130_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" .
}