Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion> ?p ?o ?g. }
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- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion type Assertion NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_head.
- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion description "[We sequenced the MLH1/MSH2 coding and promoter core regions in CRC patients diagnosed below age 40, and/or with multiple primary cancers or familial cancer clustering suggestive of HNPCC, and correlated deleterious mutations with clinical and tumour features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_provenance.
- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion evidence source_evidence_literature NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_provenance.
- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion SIO_000772 15996210 NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_provenance.
- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion wasDerivedFrom befree-20140225 NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_provenance.
- NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_assertion wasGeneratedBy ECO_0000203 NP592549.RA3keHDOljYjte8dtdj0RlJC_XagR22TeFQm_9fUR4XAk130_provenance.