@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8> .
@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:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_head {
  this: np:hasAssertion dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion ;
    np:hasProvenance dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance ;
    np:hasPublicationInfo dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion a np:Assertion .
  dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance a np:Provenance .
  dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion {
  miriam-gene:5781 a ncit:C16612 .
  lld:C0027819 a ncit:C7057 .
  dgn-gda:DGN7c59ef452207bf2fb43c0730a3603683 sio:SIO_000628 miriam-gene:5781 , lld:C0027819 ;
    a sio:SIO_001121 .
}
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance {
  dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion dcterms:description "[Associations between Noonan syndrome and an increased risk of some malignancies, notably leukemia and neuroblastoma, have been reported, and recent data indicate that somatic PTPN11 mutations occur in children with sporadic juvenile myelomonocytic leukemia, myelodysplasic syndrome, B-cell acute lymphoblastic leukemia, and acute myelogenous leukemia (AML).]. 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:15604238 ;
    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:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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" .
}