Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_assertion description "[Therefore, we assume that FLT3 mutations and the other genetic and chromosomal alterations may cooperate with PML-RARA in the development of APL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_assertion evidence source_evidence_literature NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_assertion SIO_000772 22562027 NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_assertion wasDerivedFrom befree-2016 NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_assertion wasGeneratedBy ECO_0000203 NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP979926.RArW7QD3NDE0GNaQzoHl1ZkDXXW3JvuiAIjBePhFV6hK0130_provenance.