Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_assertion description "[The clinical features of the patient are distinct from X-linked myopathy with excessive autophagy, infantile autophagic vacuolar myopathy and autophagic vacuolar myopathy with late-onset and multiorgan involvement (Kaneda).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_assertion evidence source_evidence_literature NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_assertion SIO_000772 17541230 NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_assertion wasDerivedFrom befree-2016 NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_assertion wasGeneratedBy ECO_0000203 NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.
- befree-2016 importedOn "2016-02-19" NP612781.RAAHaWPdRfIOji9bZsb5uHH3-HeCzxN_7ZjCIDQSvZ8JM130_provenance.