http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#head http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#assertion http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#provenance http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#assertion http://rdf.disgenet.org/resource/gda/DGN5acf6b8cc088ad335c1f6632975abd2f http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4869 http://rdf.disgenet.org/resource/gda/DGN5acf6b8cc088ad335c1f6632975abd2f http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0023467 http://rdf.disgenet.org/resource/gda/DGN5acf6b8cc088ad335c1f6632975abd2f http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#provenance http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#assertion http://purl.org/dc/terms/description [Mutations of the WT1 gene have been reported as the most common abnormality after NPM1 and FLT3 gene mutations in acute myeloid leukemia (AML), while KIT mutations are predominantly found in core-binding factor (CBF) AMLs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#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/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/21504297 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#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/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/dc/terms/created 2017-10-17T13:15:04+02:00 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP766578.RATvCauAJ44u9499Rsi-h6IfnxQJGgZI1S7MqmFtpSsHQ 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