@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_head {
  this: np:hasAssertion dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_assertion ;
    np:hasProvenance dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_provenance ;
    np:hasPublicationInfo dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_assertion a np:Assertion .
  dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_provenance a np:Provenance .
  dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_assertion {
  miriam-gene:7430 a ncit:C16612 .
  lld:C0024523 a ncit:C7057 .
  dgn-gda:DGN3d061ae1ff01724ff089045680d5079e sio:SIO_000628 miriam-gene:7430 , lld:C0024523 ;
    a sio:SIO_001121 .
}
dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_provenance {
  dgn-np:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_assertion dcterms:description "[We observe a similar loss of the subapical enrichment of Rab11a and the kinases and reduced phosphorylation of ezrin in microvillus inclusion disease, which is associated with MYO5B mutations, intestinal microvilli atrophy and malabsorption.]. 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:24413175 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP773989.RAYDpz72wEpBLlDPjp9s8vllkXq8fg4STt9IQPzgMJrDY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:28+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}