Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP466319.RAT_QuPWzh51oFqeBmH6ORlwDKGLUls2BZgk0cLPSrCF8130_provenance.