Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion> ?p ?o ?g. }
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- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion type Assertion NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_head.
- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion description "[The 657del5 mutation (Slavic mutation) was found in two of 117 carcinomas studied (1.7%) - in both cases it was present in the germline; one of these tumours showed loss of heterozygosity (LOH) for the 657del5 mutation and loss of nibrin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion evidence source_evidence_literature NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion SIO_000772 12485469 NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion wasDerivedFrom befree-20140225 NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_assertion wasGeneratedBy ECO_0000203 NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.