@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE
> .
@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:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_head
{
this:
np:hasAssertion
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion
;
np:hasProvenance
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance
;
np:hasPublicationInfo
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion
a
np:Assertion
.
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance
a
np:Provenance
.
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGNa690e5fe3d29bc73923db72ce9c6bb7a
sio:SIO_000628
miriam-gene:1917
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_provenance
{
dgn-np:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_assertion
dcterms:description
"[The significant difference in skeletal muscle mtDNA suggests that SIM or statin treatments are associated with depletion of skeletal muscle mtDNA or that patients with an underlying predisposition to SIM have lower mtDNA levels.]. 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:23312852
;
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:NP344090.RAe5GCAbs_hJZ2N91eFxpWZw04hJJdlHjOZmVuFhXUruE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}