Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion type Assertion NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_head.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion description "[Authors describe clinical, pathological, imaging and genetic findings in the first Irish family with Laing distal myopathy in whom a novel mutation in the human slow ?-myosin heavy chain (MYH7) gene has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion evidence source_evidence_literature NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion SIO_000772 25447691 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion wasDerivedFrom befree-2016 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.
- NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_assertion wasGeneratedBy ECO_0000203 NP1242244.RANdyI468hLplRysc4vqBxc-oO9ha_APQ8lSi1RlMlRts130_provenance.