Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion evidence source_evidence_literature NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion SIO_000772 17676042 NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion wasDerivedFrom befree-20150227 NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_assertion wasGeneratedBy ECO_0000203 NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP357198.RAyZXtrbHgU1JWSGyiPH_9KAcJd31V-K4KYM_rZ0eMEjQ130_provenance.