Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion type Assertion NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_head.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_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." NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion evidence source_evidence_literature NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion SIO_000772 7704558 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion wasDerivedFrom befree-20140225 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.
- NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_assertion wasGeneratedBy ECO_0000203 NP935925.RAkWa8ZknPa92X1mHlsHcafbXo92JWepWZK_gt5jOcV38130_provenance.