Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion> ?p ?o ?g. }
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- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion type Assertion NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_head.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion description "[A primary role of the ABCA4 gene in STGD1/FFM and AR CRD, together with the gene's involvement in an as-yet-unknown proportion of cases with AR RP, strengthens the idea that mutations in the ABCA4 gene could be the most frequent cause of inherited retinal dystrophy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion evidence source_evidence_literature NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion SIO_000772 10958761 NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion wasDerivedFrom befree-20140225 NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.
- NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_assertion wasGeneratedBy ECO_0000203 NP237357.RAGMtynsJZ8JqdfeS8wW_jucMeLLSFEB2dVU-Z3_8WPSg130_provenance.