Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion> ?p ?o ?g. }
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- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion type Assertion NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_head.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion evidence source_evidence_curated NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion SIO_000772 21480433 NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion wasDerivedFrom uniprot-2016 NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.
- NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_assertion wasGeneratedBy ECO_0000218 NP6599.RAadjMrBoJ8Hn3K5Rq1UBxgB8ZObbk_FZqJhCSE9ej3Hw130_provenance.