@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U> .
@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:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_head {
   this: np:hasAssertion dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_assertion ;
    np:hasProvenance dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_provenance ;
    np:hasPublicationInfo dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_assertion a np:Assertion .
  dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_provenance a np:Provenance .
  dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_assertion {
   miriam-gene:5476 a ncit:C16612 .
  lld:C0342276 a ncit:C7057 .
  dgn-gda:DGN70da5de80a4ed0d35a02e88edf456feb sio:SIO_000628 miriam-gene:5476 , lld:C0342276 ;
    a sio:SIO_001121 .
}
dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_provenance {
   dgn-np:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_assertion dcterms:description "[These markers and dinucleotide repeat markers associated with the D20S43, D20S46, D20S55, D20S75, and PLC1 loci and RFLPs at the D20S16, D20S17, D20S22, and D20S33 have been used to map the MODY locus on chromosome 20 to a 13-cM (sex averaged) interval encompassing ADA, D20S17, PPGB, D20S16, and D20S75 on the long arm of chromosome 20 and to create a genetic framework for additional genetic and physical mapping studies of the region.]. 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:8094595 ;
    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:NP899113.RAxgfg59MnqckQ3jXFwmwgn8dV_Iur8XhJ3J4TbzGN3-U130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:12+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" .
}