Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_assertion description "[Mutations in the BIN1 gene cause centronuclear myopathy, which shares some histopathological features with myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_assertion evidence source_evidence_literature NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_assertion SIO_000772 21623381 NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_assertion wasDerivedFrom befree-2016 NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_assertion wasGeneratedBy ECO_0000203 NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.
- befree-2016 importedOn "2016-02-19" NP897875.RAy_Ciyh_VUBEj3P2e-SeSB5GbeqFL7KC73PMxSgUfQsY130_provenance.