@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og> .
@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:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_head {
  this: np:hasAssertion dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion ;
    np:hasProvenance dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance ;
    np:hasPublicationInfo dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion a np:Assertion .
  dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance a np:Provenance .
  dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion {
  miriam-gene:7476 a ncit:C16612 .
  lld:C1856728 a ncit:C7057 .
  dgn-gda:DGNac4545e9ac45e131c68e2855e48c3af6 sio:SIO_000628 miriam-gene:7476 , lld:C1856728 ;
    a sio:SIO_001121 .
}
dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_provenance {
  dgn-np:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_assertion dcterms:description "[Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel (AA/RRS) phocomelia syndrome are rare autosomal recessive inherited disorders characterized by aplastic/hypoplastic nails with ectopic dorsal palms, absence of humeri, hypoplastic ulnae, and bowed short radii with the elbow joints present, shown to result from missense mutations in WNT7A (p.Ala109Thr and p.Arg292Cys).]. 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:21344627 ;
    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:NP596528.RAceObXZtoi9B0-EvXyQThCb_k_ItEwHQZWy017Ppa6Og130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:58+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" .
}