Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion> ?p ?o ?g. }
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- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion type Assertion NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_head.
- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion description "[LCA5, a rare genetic cause of leber congenital amaurosis in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_provenance.
- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion evidence source_evidence_literature NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_provenance.
- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion SIO_000772 19172513 NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_provenance.
- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion wasDerivedFrom befree-2016 NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_provenance.
- NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_assertion wasGeneratedBy ECO_0000203 NP716765.RARf6giMFzffZBvLGtN_8mEUIyYshS7g4p7EUMNUCyzMU130_provenance.