Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion> ?p ?o ?g. }
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- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion type Assertion NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_head.
- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion description "[the different biochemical assays yielded no evidence that the eight MLH3 unclassified variants (missense mutations) tested are the cause of hereditary colorectal cancer, including Lynch syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_provenance.
- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion evidence source_evidence_literature NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_provenance.
- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion SIO_000772 19156873 NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_provenance.
- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion wasDerivedFrom lhgdn-20090331 NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_provenance.
- NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_assertion wasGeneratedBy ECO_0000203 NP245098.RA14vJWnwh5ZTpW9uRkrQstXv_HnQW3tqxDU9ZaGTKbuA130_provenance.