Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_assertion description "[These results suggest a precise stepwise kinetic mechanism for hMSH2-hMSH6 functions that appears to mimic G protein switches, severely constrains models for MMR, and may partially explain the MSH2 allele frequency in Lynch syndrome or hereditary nonpolyposis colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_assertion evidence source_evidence_literature NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_assertion SIO_000772 21937421 NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_assertion wasDerivedFrom befree-2016 NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_assertion wasGeneratedBy ECO_0000203 NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP925461.RAQSAiIQV9sIlAbR3Ro4SQaKDEum9hOe5W6Wy-O3dLxsQ130_provenance.