@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug> .
@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:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_head {
  this: np:hasAssertion dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_assertion;
    np:hasProvenance dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_provenance;
    np:hasPublicationInfo dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_assertion a np:Assertion .
  
  dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_provenance a np:Provenance .
  
  dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_assertion {
  miriam-gene:123811 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNcf6a40c0ceadb95699a60bce51c7663e sio:SIO_000628 miriam-gene:123811, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_provenance {
  dgn-np:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_assertion dcterms:description
      "[Massachusetts currently offers an optional expanded newborn screening programme that tests for 20 biochemical genetic disorders in addition to the mandated newborn screening tests, including phenylketonuria (PKU) and nine other biochemical genetic 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:16435173;
    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:NP968112.RASY0qrg2vcZN0MvWYZyond0uv9DTqvT43EPF_m9YO-Ug130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:31+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" .
}