Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion> ?p ?o ?g. }
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- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion type Assertion NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_head.
- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion wasGeneratedBy ECO_0000203 NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_provenance.
- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion wasDerivedFrom befree-20150227 NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_provenance.
- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion SIO_000772 11968081 NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_provenance.
- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion evidence source_evidence_literature NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_provenance.
- NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_assertion description "[Mutations in RPGR, retinitis pigmentosa GTPase regulator, are associated with RP3 type of X-linked retinitis pigmentosa, a severe, non-syndromic form of retinal degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674478.RAk2N-aulPLe3-BV8YuZtAPtFHdPNCsm7LP6bKLrnLpQs130_provenance.