@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s> .
@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:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_head {
  this: np:hasAssertion dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_assertion;
    np:hasProvenance dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_provenance;
    np:hasPublicationInfo dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_assertion a np:Assertion .
  
  dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_provenance a np:Provenance .
  
  dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_assertion {
  miriam-gene:6611 a ncit:C16612 .
  
  lld:C0796160 a ncit:C7057 .
  
  dgn-gda:DGN0f5fa1dfbc59396fc8523acc3dde4522 sio:SIO_000628 miriam-gene:6611, lld:C0796160;
    a sio:SIO_001121 .
}

dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_provenance {
  dgn-np:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_assertion dcterms:description
      "[To investigate the mutability of the SMS, we carried out in silico analysis and in vitro experiments of the effects of amino acid substitutions at the missense mutation sites (G56, V132 and I150) that have been shown to cause SRS.]. 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:21647366;
    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:NP899944.RA_XfDUCPnr4ijZWyLW4KCt4HYIyiTP9x8vbtur03K16s130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:32+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: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" .
}