@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g
> .
@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:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_head
{
this:
np:hasAssertion
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_assertion
;
np:hasProvenance
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_provenance
;
np:hasPublicationInfo
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_assertion
a
np:Assertion
.
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_provenance
a
np:Provenance
.
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_assertion
{
miriam-gene:23417
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGN373ceb8eac31f10b8e355aeb65214d6d
sio:SIO_000628
miriam-gene:23417
,
lld:C0020615
;
a
sio:SIO_001121
.
}
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_provenance
{
dgn-np:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_assertion
dcterms:description
"[The metabolic role of malonyl CoA decarboxylase has not been fully defined, but deficiency of the enzyme has been associated with mild mental retardation, seizures, hypotonia, cardiomyopathy, vomiting, hypoglycemia, metabolic acidosis, and malonic aciduria.]. 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:9869665
;
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:NP824891.RAhQQr3KRUSXUwxQb2OQ23525-fdc7uvEgdXcVbwgUF1g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}