@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU> .
@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:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_head {
  this: np:hasAssertion dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion;
    np:hasProvenance dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_provenance;
    np:hasPublicationInfo dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion a np:Assertion .
  
  dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_provenance a np:Provenance .
  
  dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion {
  miriam-gene:7499 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGN24c8d6fa5db29d949cd7c26f1eb2a3e6 sio:SIO_000628 miriam-gene:7499, lld:C0026850;
    a sio:SIO_001121 .
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dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_provenance {
  dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion dcterms:description
      "[Analyses of 11 families with DMD and ten with BMD, informative for the Xg blood group, reinforce the conclusions of others that there is no measurable linkage between the loci for Xg and for the X-linked forms of muscular dystrophy.]. 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:6317539;
    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:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:35+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;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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