Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion> ?p ?o ?g. }
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- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion type Assertion NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_head.
- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion description "[CMT1, an inherited motor and sensory neuropathy with low nerve conduction velocities, is caused by dominantly inherited mutations in the genes of the peripheral myelin protein 22 (PMP22), myelin protein zero (MPZ/P(0)), and early growth response 2 transcription factor (EGR2/Krox-20).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_provenance.
- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion evidence source_evidence_literature NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_provenance.
- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion SIO_000772 11445635 NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_provenance.
- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion wasDerivedFrom befree-20150227 NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_provenance.
- NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_assertion wasGeneratedBy ECO_0000203 NP632427.RA16BjT9vvOedRHE2-lBnPl5HrqKKu0x5wDoMzUzL81wc130_provenance.