@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ
> .
@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:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_head
{
this:
np:hasAssertion
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_assertion
;
np:hasProvenance
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_assertion
a
np:Assertion
.
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_provenance
a
np:Provenance
.
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_assertion
{
miriam-gene:387254
a
ncit:C16612
.
lld:C0268583
a
ncit:C7057
.
dgn-gda:DGN818c712b3cdf4ae91ebba8b27e9e47cf
sio:SIO_000628
miriam-gene:387254
,
lld:C0268583
;
a
sio:SIO_001121
.
}
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_provenance
{
dgn-np:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_assertion
dcterms:description
"[One of the processing proteins, MMAA (methylmalonic aciduria type A), is implicated in the mitochondrial assembly of AdoCbl into MUT and is defective in children from the cblA complementation group of cobalamin disorders.]. 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:20876572
;
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:NP764545.RALe4PUvJENdf6fuPiWdCNNnTcHv4yvNobLbG2rO3yxWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}