Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion> ?p ?o ?g. }
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- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion type Assertion NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_head.
- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion wasGeneratedBy ECO_0000218 NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_provenance.
- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion wasDerivedFrom uniprot-2016 NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_provenance.
- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion SIO_000772 12659814 NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_provenance.
- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion evidence source_evidence_curated NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_provenance.
- NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_assertion description "[Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2607.RAkpsqoaToC3B-qK1o-1N7xNqpCpeF1_6AmWQS8lcOxYk130_provenance.