Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion type Assertion NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_head.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion description "[Two families with a retinal dystrophy were extensively phenotyped and blood was taken for mutation analysis of the RDS (all) and ROM1 (retinitis pigmentosa patients only) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion evidence source_evidence_literature NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion SIO_000772 16916875 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion wasDerivedFrom befree-20150227 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion wasGeneratedBy ECO_0000203 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.