Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_assertion description "[We, therefore, investigated individuals from families with one or more first-degree relatives with myelodysplastic syndrome/acute myeloid leukemia with wild-type RUNX1 and CEBPA, for GATA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_assertion evidence source_evidence_literature NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_assertion SIO_000772 22271902 NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_assertion wasDerivedFrom befree-2016 NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_assertion wasGeneratedBy ECO_0000203 NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP955599.RAnjA9XMK-FyZXTdaXdKtFTKczWOUOgBCK2hUsx43IsnQ130_provenance.