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- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion type Assertion NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_head.
- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion wasGeneratedBy ECO_0000203 NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.
- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion wasDerivedFrom befree-20140225 NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.
- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion SIO_000772 19339306 NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.
- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion evidence source_evidence_literature NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.
- NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_assertion description "[Inactivating mutations in the retinoid isomerase (RPE65) or lecithin:retinol acyltransferase (LRAT) genes cause Leber congenital amaurosis (LCA), a severe visual impairment in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401551.RAReQNdFTmvo1HTSnF92USiqV5DVfQUDjOZKjgZk74TxI130_provenance.