@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU> .
@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:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_head {
  this: np:hasAssertion dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_assertion;
    np:hasProvenance dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_provenance;
    np:hasPublicationInfo dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_assertion a np:Assertion .
  
  dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_provenance a np:Provenance .
  
  dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_assertion {
  miriam-gene:8291 a ncit:C16612 .
  
  lld:C0026846 a ncit:C7057 .
  
  dgn-gda:DGNe2d3ffe4a32d9132418f419f8a4e0f3b sio:SIO_000628 miriam-gene:8291, lld:C0026846;
    a sio:SIO_001121 .
}

dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_provenance {
  dgn-np:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_assertion dcterms:description
      "[Two other conditions have been shown to map to this region or to the homologous region in mouse: a gene for a form of autosomal recessive distal muscular dystrophy, Miyoshi myopathy, shows linkage to the same markers on chromosome 2p as LGMD2B, and an autosomal recessive mouse mutation mnd2, in which there is rapidly progressive paralysis and muscle atrophy, has been mapped to mouse chromosome 6 to a region showing conserved synteny with human chromosome 2p12-p13.]. 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:8617508;
    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:NP745624.RA1P9k6XhPkzc3KDh_XQ2Flrw5zvRlr6IRJ-yzePWrRqU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:32+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" .
}