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- source_evidence_literature type ECO_0000212 NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_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." NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_assertion evidence source_evidence_literature NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_assertion SIO_000772 17676042 NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_assertion wasDerivedFrom befree-20150227 NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_assertion wasGeneratedBy ECO_0000203 NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP237810.RArQbmIXbYde3DggKSZw1ZPtix3-xPiEhMpeMxjc4tvuA130_provenance.