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- source_evidence_literature type ECO_0000212 NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_assertion description "[Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_assertion evidence source_evidence_literature NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_assertion SIO_000772 22288654 NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_assertion wasDerivedFrom befree-2016 NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_assertion wasGeneratedBy ECO_0000203 NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.
- befree-2016 importedOn "2016-02-19" NP956979.RA0GLLCVZSq4WT1NKL9_ygnPDSQ7O4j5yaakve1KYUimo130_provenance.