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