Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion> ?p ?o ?g. }
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- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion type Assertion NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_head.
- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion description "[Insulin insensitivity of uncertain etiology often exists in myotonic muscular dystrophy, a multitissue, autosomal dominant disorder hypothesized to be a hereditary membrane disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_provenance.
- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion evidence source_evidence_literature NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_provenance.
- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion SIO_000772 7017735 NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_provenance.
- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion wasDerivedFrom befree-2016 NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_provenance.
- NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_assertion wasGeneratedBy ECO_0000203 NP1307477.RAariDU4nR8GWr4O2QP_upb0am6Gv8lOhlC9HwDUzgLZA130_provenance.