@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU> .
@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:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_head {
  this: np:hasAssertion dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_assertion ;
    np:hasProvenance dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_provenance ;
    np:hasPublicationInfo dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_assertion a np:Assertion .
  dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_provenance a np:Provenance .
  dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_assertion {
  miriam-gene:1936 a ncit:C16612 .
  lld:C0026847 a ncit:C7057 .
  dgn-gda:DGNc29ae6c1ff39d643a9448f6ebdbf5950 sio:SIO_000628 miriam-gene:1936 , lld:C0026847 ;
    a sio:SIO_001121 .
}
dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_provenance {
  dgn-np:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_assertion dcterms:description "[Potentially interesting novel loci, including EEF1D, a translation elongation factor involved in the delivery of aminoacyl tRNAs to the ribosome (a process which has previously been implicated in genetic studies of spinal muscular atrophy) were identified but must be treated with caution due to concerns surrounding genomic location and platform suitability.]. 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:19997636 ;
    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:NP566847.RAY5L-qWoksUn_sAhRHEf2QqhZ2PVkIJsB4J1od1uDDYU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:42+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" .
}