Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP209778.RAlvyuNi0LIVfNXqdJxRcfrXWVz1n79PxsFDO3jyJ2qyo130_provenance.