@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_head {
  this: np:hasAssertion dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_assertion;
    np:hasProvenance dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_provenance;
    np:hasPublicationInfo dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_assertion a np:Assertion .
  
  dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_provenance a np:Provenance .
  
  dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_assertion {
  miriam-gene:4594 a ncit:C16612 .
  
  lld:C0276096 a ncit:C7057 .
  
  dgn-gda:DGN2b322eb038e65c2be9d81709822cd49e sio:SIO_000628 miriam-gene:4594, lld:C0276096;
    a sio:SIO_001121 .
}

dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_provenance {
  dgn-np:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_assertion dcterms:description
      "[Methylmalonic acidemia (MMA) can be caused by mutations in the gene coding for the methylmalonyl CoA mutase (MCM) apoenzyme or by mutations in genes required for provision of its adenosylcobalamin cofactor.]. 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:1968706;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP758082.RAtE7i_E0VpU38KpKFeOi4NAT9KJcaqrdwfA-yda2uAbE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}