@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg
> .
@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:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_head
{
this:
np:hasAssertion
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_assertion
;
np:hasProvenance
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_assertion
a
np:Assertion
.
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_provenance
a
np:Provenance
.
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_assertion
{
miriam-gene:6992
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN5870c8b0dc5ab30f9a8e4aa3864a8ec4
sio:SIO_000628
miriam-gene:6992
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_provenance
{
dgn-np:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_assertion
dcterms:description
"[The confirmation of the complex II inhibitor 3-nitropropionic acid as a toxin model for Huntington's disease, together with the demonstration of reduced mitochondrial function in Huntington's disease caudate, supports the proposition that mutant huntingtin may exert its effect through an abnormality of energy metabolism.]. 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:8858182
;
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:NP303414.RAjgmAxpFp_t0rrk8ivb5usOYPB8ZrtiaCvofZGQyILwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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" .
}