@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY> .
@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:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_head {
  this: np:hasAssertion dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion;
    np:hasProvenance dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance;
    np:hasPublicationInfo dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion a np:Assertion .
  
  dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance a np:Provenance .
  
  dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion {
  miriam-gene:4359 a ncit:C16612 .
  
  lld:C0270912 a ncit:C7057 .
  
  dgn-gda:DGN2d79f4bb1af38794f240b50f704fdb58 sio:SIO_000628 miriam-gene:4359, lld:C0270912;
    a sio:SIO_001121 .
}

dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_provenance {
  dgn-np:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_assertion dcterms:description
      "[Identifying molecular pathways involved in early and late onset CMT1B will be crucial to understand how MPZ mutations cause CMT1B so that rational therapies for both early and late onset neuropathies can be developed.]. 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:16414078;
    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:NP307984.RAClQATguM5EQXxwcTw3Xcubdgp09qfpkboKtttxnJlJY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}