Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion> ?p ?o ?g. }
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- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion type Assertion NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_head.
- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_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." NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_provenance.
- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion evidence source_evidence_literature NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_provenance.
- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion SIO_000772 7704558 NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_provenance.
- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion wasDerivedFrom befree-2016 NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_provenance.
- NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_assertion wasGeneratedBy ECO_0000203 NP1319020.RAyYoUO3T0fpXtVuQs3BsHSuKSlpfAsVPZcRlQ0dSwTPI130_provenance.