@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E> .
@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:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_head {
  this: np:hasAssertion dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion;
    np:hasProvenance dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance;
    np:hasPublicationInfo dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion a np:Assertion .
  
  dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance a np:Provenance .
  
  dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion {
  miriam-gene:4070 a ncit:C16612 .
  
  lld:C0010036 a ncit:C7057 .
  
  dgn-gda:DGN06c5b997ee3e052be1da7ea8b79430e4 sio:SIO_000628 miriam-gene:4070, lld:C0010036;
    a sio:SIO_001121 .
}

dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance {
  dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion dcterms:description
      "[Although gelatinous corneal dystrophy has previously been mapped to chromosome 1p and seems to be associated with mutations in the M1S1 gene, molecular genetic studies have been limited to Japanese patients.]. 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:12107443;
    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:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}