Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion> ?p ?o ?g. }
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- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion type Assertion NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_head.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion description "[A mutation in this gene causes X-linked cone dystrophy/type of hereditary retinal degeneration is distinct from retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion evidence source_evidence_literature NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion SIO_000772 11875055 NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion wasDerivedFrom lhgdn-20090331 NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.
- NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_assertion wasGeneratedBy ECO_0000203 NP122319.RALS4iFWHgqfRzcM4_-btga9TlZchzbULLJR9-4QlDkdY130_provenance.