@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU> .
@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/v3.0.0/void/> .

dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_head {
  this: np:hasAssertion dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_assertion;
    np:hasProvenance dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_provenance;
    np:hasPublicationInfo dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_assertion a np:Assertion .
  
  dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_provenance a np:Provenance .
  
  dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_assertion {
  miriam-gene:34 a ncit:C16612 .
  
  lld:C0220710 a ncit:C7057 .
  
  dgn-gda:DGN56295c173485744f938e08bdb64a1bb7 sio:SIO_000628 miriam-gene:34, lld:C0220710;
    a sio:SIO_001121 .
}

dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_provenance {
  dgn-np:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_assertion dcterms:description
      "[Currently available information from screening studies on the frequency of detection of MCADD in newborns, as well as the frequency of homozygotes for the common mutation in the ACADM gene, is summarized.]. 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:16617240;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP220357.RAC0GOyaa3BWRcZVZN5xRrxWa_LfIEQnNokmJ23SbSlrU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:45+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}