@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8> .
@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:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_head {
  this: np:hasAssertion dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_assertion;
    np:hasProvenance dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_provenance;
    np:hasPublicationInfo dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_assertion a np:Assertion .
  
  dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_provenance a np:Provenance .
  
  dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_assertion {
  miriam-gene:4914 a ncit:C16612 .
  
  lld:C0238462 a ncit:C7057 .
  
  dgn-gda:DGNdcaa3ad314a2b3a077ba631ace45f079 sio:SIO_000628 miriam-gene:4914, lld:C0238462;
    a sio:SIO_001121 .
}

dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_provenance {
  dgn-np:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_assertion dcterms:description
      "[Although we did not find any somatic mutations of NTRK1 in sporadic MTC, the single-strand conformational polymorphism conditions reported here, together with the knowledge of the frequency of various sequence variants, may help in future mutation analyses of DNA from other neural and nonneural tissues.]. 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:10443680;
    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:NP188702.RA7ROo6H4THpPyT9hD8dKjhdk96rUEh5BhQLT6UeKa4Z8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}