@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E
> .
@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:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_head
{
this:
np:hasAssertion
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_assertion
;
np:hasProvenance
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_assertion
a
np:Assertion
.
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_provenance
a
np:Provenance
.
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_assertion
{
miriam-gene:5095
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGN717886454c5227976984f84035d89e8d
sio:SIO_000628
miriam-gene:5095
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_provenance
{
dgn-np:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_assertion
dcterms:description
"[The inherited metabolic disease propionic acidemia (PA) can result from mutations in either of the genes PCCA or PCCB, which encode the alpha and beta subunits, respectively, of the mitochondrial enzyme propionyl CoA-carboxylase.]. 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:10101253
;
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:NP323734.RApoaxtSNrDEygPpiSkAJUfiPt44CqDQ3a3L7mTWx2M2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}