@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8
> .
@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:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_head
{
this:
np:hasAssertion
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_assertion
;
np:hasProvenance
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_provenance
;
np:hasPublicationInfo
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_assertion
a
np:Assertion
.
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_provenance
a
np:Provenance
.
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_assertion
{
miriam-gene:490
a
ncit:C16612
.
lld:C0231528
a
ncit:C7057
.
dgn-gda:DGN3efe007aabace394573ce43527115026
sio:SIO_000628
miriam-gene:490
,
lld:C0231528
;
a
sio:SIO_001121
.
}
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_provenance
{
dgn-np:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_assertion
dcterms:description
"[The candidate genes COQ2, ATP2B1, and DMPK, representing pathways involved in myocellular energy transfer, calcium homeostasis, and myotonic dystonia, respectively, were validated as markers for the common myalgia observed in patients receiving statin therapy.]. 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:21868014
;
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:NP835733.RApnPYbwWbVdlsSl_FcsSv65_76AsI4h26wq-rOjd_ZR8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}