Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion> ?p ?o ?g. }
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- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion type Assertion NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_head.
- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion description "[Mutations in FLCN are also responsible for Birt-Hogg-Dub� (BHD) syndrome (a dominantly inherited disease characterized by benign skin tumors, PSP, and diverse types of renal cancer) and, rarely, are detected in sporadic renal and colorectal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion evidence source_evidence_literature NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion SIO_000772 15657874 NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion wasDerivedFrom befree-20140225 NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_assertion wasGeneratedBy ECO_0000203 NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.