@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU> .
@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:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_head {
  this: np:hasAssertion dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_assertion;
    np:hasProvenance dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_provenance;
    np:hasPublicationInfo dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_assertion a np:Assertion .
  
  dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_provenance a np:Provenance .
  
  dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_assertion {
  miriam-gene:5894 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGNe42bd4deada57658ca27122c1e4164b4 sio:SIO_000628 miriam-gene:5894, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_provenance {
  dgn-np:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_assertion dcterms:description
      "[Cells transfected with constructs containing Noonan syndrome-associated RAF1 mutations showed increased in vitro kinase and ERK activation, and zebrafish embryos with morpholino knockdown of raf1 demonstrated the need for raf1 for the development of normal myocardial structure and function.]. 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:17603482;
    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:NP28096.RAMCUIqqignS3sn3zkBngbYo5WwDIwakx28gXNNOA8xtU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:12+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" .
}