@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM> .
@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:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_head {
  this: np:hasAssertion dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_assertion;
    np:hasProvenance dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_provenance;
    np:hasPublicationInfo dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_assertion a np:Assertion .
  
  dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_provenance a np:Provenance .
  
  dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_assertion {
  miriam-gene:11258 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGN0b3162f1298696e1aa66603ca3d0e758 sio:SIO_000628 miriam-gene:11258, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_provenance {
  dgn-np:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_assertion dcterms:description
      "[These findings indicate that loss of chromosomal material in the region of 9p21-p22 is closely associated with lymphomatous ALL; by analogy with retinoblastoma, in which gene deletions are associated with an enzyme deficiency, this disease may be related to the loss of the enzyme methylthioadenosine phosphorylase, previously reported in some of these patients.]. 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:3925340;
    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:NP154222.RAmauDfJmw0EwyjC3Ej0kCS7G67AeHFqOcF5VblxOgqSM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}