Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion> ?p ?o ?g. }
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- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion type Assertion NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_head.
- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.
- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion evidence source_evidence_literature NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.
- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion SIO_000772 11535114 NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.
- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion wasDerivedFrom befree-20140225 NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.
- NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_assertion wasGeneratedBy ECO_0000203 NP583550.RAGyg-0KyOBGohrOpE5tKNvYyeXZ-nqN0b9Jb0QQBC-CA130_provenance.