Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion type Assertion NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_head.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_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." NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_provenance.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion evidence source_evidence_literature NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_provenance.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion SIO_000772 11445635 NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_provenance.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion wasDerivedFrom befree-20140225 NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_provenance.
- NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_assertion wasGeneratedBy ECO_0000203 NP328410.RA-_mWd3KD15ddxB6GaWrMO7oX2fc5-Yemt3t0jIcfYPE130_provenance.