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- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion type Assertion NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_head.
- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion wasGeneratedBy ECO_0000203 NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.
- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion wasDerivedFrom befree-20150227 NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.
- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion SIO_000772 11535114 NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.
- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_assertion evidence source_evidence_literature NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.
- NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_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." NP632552.RA-ul88yr5byIYtpCzScuONe_-Vn-j_jaZW_klAYNDhwY130_provenance.