@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o
> .
@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:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_head
{
this:
np:hasAssertion
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_assertion
;
np:hasProvenance
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_assertion
a
np:Assertion
.
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_provenance
a
np:Provenance
.
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_assertion
{
miriam-gene:166785
a
ncit:C16612
.
lld:C0268583
a
ncit:C7057
.
dgn-gda:DGNe03acdb8c20b4a8fe08febf44ba986a0
sio:SIO_000628
miriam-gene:166785
,
lld:C0268583
;
a
sio:SIO_001121
.
}
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_provenance
{
dgn-np:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_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:NP910177.RAlqVfttOXZN_hjyiaEz9dz7OPojYyLv8gbOcD28F9H8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}