Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion> ?p ?o ?g. }
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- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion type Assertion NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_head.
- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion description "[Welander distal myopathy (WDM) is an autosomal dominant myopathy with late-adult onset characterized by slow progression of distal muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_provenance.
- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion evidence source_evidence_literature NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_provenance.
- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion SIO_000772 10482271 NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_provenance.
- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion wasDerivedFrom befree-2016 NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_provenance.
- NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_assertion wasGeneratedBy ECO_0000203 NP262677.RAeI5DtB7EeDSkfieB64n-Jjn0lcfACWzm0vpylpx93sM130_provenance.