@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI
> .
@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:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_head
{
this:
np:hasAssertion
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_assertion
;
np:hasProvenance
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_assertion
a
np:Assertion
.
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_provenance
a
np:Provenance
.
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_assertion
{
miriam-gene:7402
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN3e46147270cdb48e9475f7a44adec5bf
sio:SIO_000628
miriam-gene:7402
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_provenance
{
dgn-np:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_assertion
dcterms:description
"[The increase in Drp1, Fis1 and CypD and the decrease in Mfn1 and Mfn2 may be responsible for abnormal mitochondrial dynamics that we found in the cortex of HD patients, and may contribute to neuronal damage in HD patients.]. 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:21257639
;
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:NP368579.RAm4dugR2v6C6R1mmi_wxg5Kc2Wv0UaoCQT-eac9k5lOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}