@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_head {
  this: np:hasAssertion dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_assertion;
    np:hasProvenance dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_provenance;
    np:hasPublicationInfo dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_assertion a np:Assertion .
  
  dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_provenance a np:Provenance .
  
  dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_assertion {
  miriam-gene:6607 a ncit:C16612 .
  
  lld:C0026847 a ncit:C7057 .
  
  dgn-gda:DGNe29ff0564d28a6f63b365bb471440b02 sio:SIO_000628 miriam-gene:6607, lld:C0026847;
    a sio:SIO_001121 .
}

dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_provenance {
  dgn-np:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_assertion dcterms:description
      "[We also show that the incidence of NAIP deletion is higher in the more severe SMA cases and the dual deletion of the SMN1 and NAIP genes are more common in Saudi SMA type I patients compared with patients of other ethnic groups.]. 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:14578966;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP418303.RA7RcBxagkc28pZa65Fz9AeF4Hx2q1CTqe4cCg7BiqXs8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:54+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}