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- source_evidence_literature type ECO_0000212 NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_assertion description "[Our results suggest that mutations in BIN1 cause centronuclear myopathy by interfering with remodeling of T tubules and/or endocytic membranes, and that the functional interaction between BIN1 and DNM2 is necessary for normal muscle function and positioning of nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_assertion evidence source_evidence_literature NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_assertion SIO_000772 17676042 NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_assertion wasDerivedFrom befree-2016 NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_assertion wasGeneratedBy ECO_0000203 NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.
- befree-2016 importedOn "2016-02-19" NP623589.RAXLLKlKJMsZGTdB49lT3mfeC-G_ALiDUpCkXVbLauAaM130_provenance.