Matches in Nanopublications for { ?s ?p "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_assertion description "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679444.RA6oE9uBR0PJUhe4bauPLQPxgZnlArb5swM8IYHfr4xv4130_provenance.
- assertion description "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_assertion description "[Abnormalities of peripheral myelin protein 22 (PMP-22) account for dominantly inherited HMSN type I in approximately 90% of families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311613.RA5GP1zFwoPosj8u8B3WaMpiOiIp_buWWsvy3b2kkSX0o130_provenance.