Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion> ?p ?o ?g. }
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- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion type Assertion NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_head.
- 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.
- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion evidence source_evidence_literature NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_provenance.
- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion SIO_000772 12136241 NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_provenance.
- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion wasDerivedFrom befree-20140225 NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_provenance.
- NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_assertion wasGeneratedBy ECO_0000203 NP168140.RACDMBXo4M5Tpo3lg-66AMi2gHtFBzEmQl1pe8QqiqqYc130_provenance.