@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE> .
@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:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_head {
  this: np:hasAssertion dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_assertion;
    np:hasProvenance dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_provenance;
    np:hasPublicationInfo dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_assertion a np:Assertion .
  
  dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_provenance a np:Provenance .
  
  dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_assertion {
  miriam-gene:6607 a ncit:C16612 .
  
  lld:C0270971 a ncit:C7057 .
  
  dgn-gda:DGNbe8fc9494bb1674a156be2e58d106be3 sio:SIO_000628 miriam-gene:6607, lld:C0270971;
    a sio:SIO_001121 .
}

dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_provenance {
  dgn-np:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_assertion dcterms:description
      "[To study the clinical profile of paralytic floppy infants undertaking available investigations and detect the frequency of exon7 of survival motor neuron (SMNT) gene deletion among the spinal muscular atrophy (SMA) cases.]. 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:11721063;
    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:NP337379.RATd1BpTSwqcb0y5WYQ786uFmmC0J3eWrSdOYRsHBxnXE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:18+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" .
}