Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_assertion description "[Inactivating or dominant-negative mutations in the RUNX1 gene have been also identified in pedigrees of familial platelet disorders with a variable propensity to develop acute myeloid leukemia (FPD/AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_assertion evidence source_evidence_literature NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_assertion SIO_000772 21725049 NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_assertion wasDerivedFrom befree-20150227 NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_assertion wasGeneratedBy ECO_0000203 NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284901.RAFbWCOx7aQBH11-PW8sX50hEO7z-dcPpS3NhSJKHqGb4130_provenance.