@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw
> .
@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:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_head
{
this:
np:hasAssertion
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_assertion
;
np:hasProvenance
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_provenance
;
np:hasPublicationInfo
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_assertion
a
np:Assertion
.
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_provenance
a
np:Provenance
.
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_assertion
{
miriam-gene:8604
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNc592fbcf78a5af11cb1c96a4f1bbdaa7
sio:SIO_000628
miriam-gene:8604
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_provenance
{
dgn-np:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_assertion
dcterms:description
"[We conclude that while mitochondrial dysfunction may be one of the most common medical conditions associated with autism, variation at the SLC25A12 gene does not explain the high frequency of mitochondrial dysfunction markers and is not associated with autism in this sample of autistic 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:17151801
;
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:NP635859.RAkh9Vty9vFt7of99ocw0ma2c9KjMmSzBnY6OOiw3RyLw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}