@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc> .
@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:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_head {
  this: np:hasAssertion dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion;
    np:hasProvenance dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance;
    np:hasPublicationInfo dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion a np:Assertion .
  
  dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance a np:Provenance .
  
  dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion {
  miriam-gene:25981 a ncit:C16612 .
  
  lld:C0022521 a ncit:C7057 .
  
  dgn-gda:DGNe75739402458afa8bd4136401e6a0d94 sio:SIO_000628 miriam-gene:25981, lld:C0022521;
    a sio:SIO_001121 .
}

dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance {
  dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion dcterms:description
      "[The phenotype of MDHC7(-/-) mice is similar to that observed in some patients suffering from PCD, and our data strongly suggest that in some patients this disease could be due to mutations in the homologous human gene DNAH1 (HDHC7).]. 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:11371505;
    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:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:09+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" .
}