Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion> ?p ?o ?g. }
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- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion type Assertion NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_head.
- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion description "[31 different germline FH mutations in 56 families with Hereditary leiomyomatosis and renal cell cancer (HLRCC) (20 missense, eight frameshifts, two nonsense, and one splice site) was indentified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_provenance.
- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion evidence source_evidence_literature NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_provenance.
- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion SIO_000772 15937070 NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_provenance.
- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion wasDerivedFrom lhgdn-20090331 NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_provenance.
- NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_assertion wasGeneratedBy ECO_0000203 NP151697.RAlryzqjh4AYlhoV6HH50x-5w1KN-qyGmr4ToLBamVxHc130_provenance.