Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_assertion description "[Oncogenic gain-of-function mutations in NOTCH1 commonly occur in human T-cell lymphoblastic leukemia/lymphoma and B-cell chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_assertion evidence source_evidence_literature NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_assertion SIO_000772 22006338 NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_assertion wasDerivedFrom befree-20150227 NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_assertion wasGeneratedBy ECO_0000203 NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP595237.RAneXaH6EWNY-8ZWaJICl_sHLHm0BjL1YvSgC7I6I1WTQ130_provenance.