Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion> ?p ?o ?g. }
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- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion type Assertion NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_head.
- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion wasGeneratedBy ECO_0000203 NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_provenance.
- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion wasDerivedFrom befree-20150227 NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_provenance.
- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion SIO_000772 8045710 NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_provenance.
- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion evidence source_evidence_literature NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_provenance.
- NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_assertion description "[Patients from two families, one with a mutation in codon 167 (Gly167Asp) leading to macular degeneration and another with a mutation in codon 210 (Pro210Ser) leading to retinitis pigmentosa, were studied with clinical examinations and measurements of rod and cone sensitivities and dark adaptation, electroretinography, and rhodopsin levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671916.RA5LCKvOIl21K6QyMCIJoZ4GYfTTpg6mY0Kv6a5XCiIiU130_provenance.