Matches in Nanopublications for { ?s ?p "[Inactivating mutations in the TSC2 gene, consisting of 41coding exons in 40 kb on 16p13, cause the hamartoma syndrome tuberous sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion description "[Inactivating mutations in the TSC2 gene, consisting of 41coding exons in 40 kb on 16p13, cause the hamartoma syndrome tuberous sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_provenance.
- NP408267.RACqlUNGO_zVRI7j-LwqMB2LVNZWvP0n85aWyhRPOldaI130_assertion description "[Inactivating mutations in the TSC2 gene, consisting of 41coding exons in 40 kb on 16p13, cause the hamartoma syndrome tuberous sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408267.RACqlUNGO_zVRI7j-LwqMB2LVNZWvP0n85aWyhRPOldaI130_provenance.