Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion> ?p ?o ?g. }
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- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion type Assertion NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_head.
- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion description "[Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_provenance.
- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion evidence source_evidence_curated NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_provenance.
- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion SIO_000772 7704558 NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_provenance.
- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion wasDerivedFrom uniprot-20130724 NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_provenance.
- NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_assertion wasGeneratedBy ECO_0000218 NP5456.RAY48QfpkH9Wkq5OVGozgLDd8dBOEARl0sM5bMonfqZV0130_provenance.