@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY> .
@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/v4.0.0/void/> .

dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_head {
  this: np:hasAssertion dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion;
    np:hasProvenance dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance;
    np:hasPublicationInfo dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion a np:Assertion .
  
  dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance a np:Provenance .
  
  dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion {
  miriam-gene:8036 a ncit:C16612 .
  
  lld:C0028326 a ncit:C7057 .
  
  dgn-gda:DGN935a389025ed57cbcf824ce9fb4b8e16 sio:SIO_000628 miriam-gene:8036, lld:C0028326;
    a sio:SIO_001121 .
}

dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_provenance {
  dgn-np:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_assertion dcterms:description
      "[In order to understand the contribution of SHOC2 mutations to the clinical manifestations of Noonan syndrome and related disorders, we analyzed SHOC2 in 92 patients with Noonan syndrome and related disorders who did not exhibit PTPN11, KRAS, HRAS, BRAF, MAP2K1/2, SOS1 or RAF1 mutations.]. 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:20882035;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP842733.RA3-UMjTx62Zr0UR3FGHrrDtH3p1fgiteoT_Kog8zX1tY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:07+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}