Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_assertion description "[These findings confirm that germline GATA2 mutations predispose to familial myelodysplastic syndrome/acute myeloid leukemia, and that monosomy 7 and ASXL1 mutations may be recurrent secondary genetic abnormalities triggering overt malignancy in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_assertion evidence source_evidence_literature NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_assertion SIO_000772 22271902 NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_assertion wasDerivedFrom befree-20140225 NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_assertion wasGeneratedBy ECO_0000203 NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP222907.RAeRV5T6we0S3MqCAbnIT-EHmsU49PpPhpfh8F4SWTEYg130_provenance.