Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion> ?p ?o ?g. }
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- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion type Assertion NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_head.
- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_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." NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_provenance.
- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion evidence source_evidence_literature NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_provenance.
- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion SIO_000772 19156873 NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_provenance.
- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion wasDerivedFrom lhgdn-20090331 NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_provenance.
- NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_assertion wasGeneratedBy ECO_0000203 NP106412.RAlifzmu3UFTt_RgXKl8gZVd7vcP6oT1BYV11Hmjgjqr4130_provenance.