Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion> ?p ?o ?g. }
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- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion type Assertion NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_head.
- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion description "[To describe in detail the characteristic clinical phenotype and electrophysiological features of Severe Early Childhood Onset Retinal Dystrophy (SECORD) caused by mutation of RPE65.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.
- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion evidence source_evidence_literature NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.
- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion SIO_000772 20811047 NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.
- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion wasDerivedFrom befree-20140225 NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.
- NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_assertion wasGeneratedBy ECO_0000203 NP445198.RAWKBfI35WgjaPi1zCcdyYw6Bi1cQ9nUVkM1wcQz3agyE130_provenance.