@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4> .
@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:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_head {
  this: np:hasAssertion dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion;
    np:hasProvenance dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance;
    np:hasPublicationInfo dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion a np:Assertion .
  
  dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance a np:Provenance .
  
  dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion {
  miriam-gene:4359 a ncit:C16612 .
  
  lld:C0027888 a ncit:C7057 .
  
  dgn-gda:DGN632fc4e4cd366c95160a3677ca2e12ef sio:SIO_000628 miriam-gene:4359, lld:C0027888;
    a sio:SIO_001121 .
}

dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_provenance {
  dgn-np:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_assertion dcterms:description
      "[We have restudied two clinically typical Charcot-Marie-Tooth neuropathy type 1 (CMT1; also known as hereditary motor and sensory neuropathy 1) pedigrees that were previously reported to be unlinked to the regions of proximal chromosome 1q and chromosome 17p by multipoint linkage analyses.]. 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:1407588;
    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:NP543826.RAovbYW6cQWMB-qWXw1yRVU8qYOnxBCoPICEm6J_ozHZ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:28+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" .
}