@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow> .
@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:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_head {
  this: np:hasAssertion dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_assertion;
    np:hasProvenance dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_provenance;
    np:hasPublicationInfo dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_assertion a np:Assertion .
  
  dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_provenance a np:Provenance .
  
  dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_assertion {
  miriam-gene:7417 a ncit:C16612 .
  
  lld:C0039075 a ncit:C7057 .
  
  dgn-gda:DGN93ceea284e88486b9ee4dbe21dc3d02d sio:SIO_000628 miriam-gene:7417, lld:C0039075;
    a sio:SIO_001121 .
}

dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_provenance {
  dgn-np:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_assertion dcterms:description
      "[POR deletion occurred earlier in forelimbs than in hind limbs, leading additionally to soft tissue syndactyly and loss of wrist elements and phalanges due to changes in growth, cell death, and skeletal segmentation.]. 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:19273610;
    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:NP518785.RAjano9uSKMELlPhPrL-tjc2Y3k3NfWYB4LJtrYzKpZow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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" .
}