@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI> .
@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:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_head {
  this: np:hasAssertion dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion ;
    np:hasProvenance dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance ;
    np:hasPublicationInfo dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion a np:Assertion .
  dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance a np:Provenance .
  dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion {
  miriam-gene:5077 a ncit:C16612 .
  lld:C3266898 a ncit:C7057 .
  dgn-gda:DGNf29ab81dd127a7b0d63acd5031e3fe94 sio:SIO_000628 miriam-gene:5077 , lld:C3266898 ;
    a sio:SIO_001121 .
}
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance {
  dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion dcterms:description "[The structure elucidates the role of serine 50 in selection of the CG sequence immediately 3' of the TAAT motif by PAX class homeodomains and provides insights into the molecular mechanisms by which certain Waardenburg syndrome-associated missense mutations could destabilize the fold of the PAX3 homeodomain whereas others could affect its interaction with DNA.]. 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:19199574 ;
    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:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:59+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" .
}