@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY> .
@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:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_head {
  this: np:hasAssertion dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_assertion;
    np:hasProvenance dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_provenance;
    np:hasPublicationInfo dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_assertion a np:Assertion .
  
  dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_provenance a np:Provenance .
  
  dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_assertion {
  miriam-gene:260402 a ncit:C16612 .
  
  lld:C0700208 a ncit:C7057 .
  
  dgn-gda:DGNe81e4ae3fd14cd02271b2145b2f276be sio:SIO_000628 miriam-gene:260402, lld:C0700208;
    a sio:SIO_001121 .
}

dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_provenance {
  dgn-np:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_assertion dcterms:description
      "[Our objectives were to quantify the genetic effect in AIS, determine the expressivity and penetrance of AIS in large family groupings, and examine larger scoliosis pedigrees for evidence of multiple genes.]. 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:16540873;
    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:NP455028.RAV9TQLGGfFRDpxyOuFrZZctBtIkTssqLAU0G3aETchmY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:31+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" .
}