http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#head http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#provenance http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://rdf.disgenet.org/resource/gda/DGN654b23bdf0b9d55111b7823792726ccb http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2187 http://rdf.disgenet.org/resource/gda/DGN654b23bdf0b9d55111b7823792726ccb http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0023449 http://rdf.disgenet.org/resource/gda/DGN654b23bdf0b9d55111b7823792726ccb http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#provenance http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://purl.org/dc/terms/description [Mutations have also been found with lower frequency in other FAB subtype AML (6 cases), in myeloproliferative disorders (6 cases), in myelodysplastic syndrome (3 cases) and rarely in acute lymphoblastic leukemia (1 case).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12529654 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/dc/terms/created 2017-10-17T13:12:38+02:00 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP386512.RAxloRyG9QhEbOirqawCm8KtyR96CFZuTk1bcEv8ZlL3Y http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0