Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_assertion description "[Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_assertion evidence source_evidence_literature NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_assertion SIO_000772 15017103 NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_assertion wasDerivedFrom befree-2016 NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_assertion wasGeneratedBy ECO_0000203 NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.
- befree-2016 importedOn "2016-02-19" NP435418.RA7CnaYkcxetW5Zy8l7SC21zJbT8zus0LJOpLjlV_kbh8130_provenance.