Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion> ?p ?o ?g. }
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- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion type Assertion NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_head.
- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion description "[Complete or partial gene deletions were identified in seven cases for hMSH2 (5.7% of mutation-negative HNPCC; 4.3% of all HNPCC), no cases for hMLH1 and six cases for APC (25% of mutation negative FAP; 8% of all FAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_provenance.
- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion evidence source_evidence_literature NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_provenance.
- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion SIO_000772 15475941 NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_provenance.
- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion wasDerivedFrom befree-2016 NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_provenance.
- NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_assertion wasGeneratedBy ECO_0000203 NP463978.RAK9g_POE8w4--dFRsv538KxPP2NDRAZDTkjb9tCSOnR0130_provenance.