@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0> .
@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:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_head {
  this: np:hasAssertion dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_assertion;
    np:hasProvenance dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_provenance;
    np:hasPublicationInfo dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_assertion a np:Assertion .
  
  dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_provenance a np:Provenance .
  
  dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_assertion {
  miriam-gene:1292 a ncit:C16612 .
  
  lld:C2827469 a ncit:C7057 .
  
  dgn-gda:DGNd414fee4bb04d49f2ddb0642a9ebcba2 sio:SIO_000628 miriam-gene:1292, lld:C2827469;
    a sio:SIO_001121 .
}

dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_provenance {
  dgn-np:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_assertion dcterms:description
      "[Motor and sensory nerve conduction velocities (NCVs) and needle electromyography (EMG) results were reviewed in 26 children with different types of congenital muscular dystrophy (CMD), including patients with mutations in the genes LAMA2, FKRP, and COL6A2.]. 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:14755496;
    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:NP704225.RAW1-WnZbMNGEIRJtJdSnykF3fAjP3oAmo8VY0uKZLMR0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}