Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_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." NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_assertion evidence source_evidence_literature NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_assertion SIO_000772 17676042 NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_assertion wasDerivedFrom befree-2016 NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_assertion wasGeneratedBy ECO_0000203 NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP623586.RAgjBGRXIoqwDLG6LxoAeWJDD_-sP6_WWNmc1yRG0dVFQ130_provenance.