Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP527072.RAR8cYm6_bKABjpC6ByE76fBr9rODoun-xi3Pyty9J-yo130_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." NP527072.RAR8cYm6_bKABjpC6ByE76fBr9rODoun-xi3Pyty9J-yo130_provenance.
• 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.
• NP338873.RA6selgLfDwXjic9HHpmLuPREcPY9gWkbEIIwscyY4bfc130_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." NP338873.RA6selgLfDwXjic9HHpmLuPREcPY9gWkbEIIwscyY4bfc130_provenance.
• 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." provenance.
• NP371296.RATgK2jXOhi32JEGjxIlb3kYqdWVnrPasxj7wAc7xLhyg130_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." NP371296.RATgK2jXOhi32JEGjxIlb3kYqdWVnrPasxj7wAc7xLhyg130_provenance.
• 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." provenance.
• 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." provenance.
• NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_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." NP323379.RABvl_fosH5F_F8qB0yelpEl_CKoGhw3gpXnrrXiDbBQU130_provenance.
• NP323377.RAecnAxizbNmN_IlrOpgrb5RcrxhI7Ti-0ts8nkbTtZb4130_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." NP323377.RAecnAxizbNmN_IlrOpgrb5RcrxhI7Ti-0ts8nkbTtZb4130_provenance.
• NP568226.RAPCzWm2fnfefU48J642ipd7fCfXKFdLGGP_7Etl9H0rM130_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." NP568226.RAPCzWm2fnfefU48J642ipd7fCfXKFdLGGP_7Etl9H0rM130_provenance.
• 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.
• NP323378.RA_Y8g3V3nWdtzlIIStR5VJmmeGlMatB7YglEDAqV81ho130_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." NP323378.RA_Y8g3V3nWdtzlIIStR5VJmmeGlMatB7YglEDAqV81ho130_provenance.