@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo> .
@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 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:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_head {
  this: np:hasAssertion dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_assertion;
    np:hasProvenance dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_provenance;
    np:hasPublicationInfo dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_assertion a np:Assertion .
  
  dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_provenance a np:Provenance .
  
  dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_assertion {
  miriam-gene:5781 a ncit:C16612 .
  
  lld:C0014084 a ncit:C7057 .
  
  dgn-gda:DGN9627bd2c1f6c574079d51413251bf854 sio:SIO_000628 miriam-gene:5781, lld:C0014084;
    a sio:SIO_001121 .
}

dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_provenance {
  dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_assertion dct:description
      "[We conclude that heterozygous loss-of-function mutations in PTPN11 are a frequent cause of MC, that lesions in patients with MC appear to arise following a `second hit,` that MC may be locus heterogeneous since 1 familial and 5 sporadically occurring cases lacked obvious disease-causing PTPN11 mutations, and that PTPN11 mutations are not a common cause of Ollier disease or Maffucci syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:21533187;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP27907.RAmgGpli3TFy30AMuos4o5v9cfv7c6sst5z_DhvKVuUTo130_publicationInfo {
  this: dct:created "2014-10-02T12:32:11+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}