Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_assertion description "[The evidences of our investigations show that MLH1 and MSH2 gene mutations have an equivalent etiopathological role both for Lynch syndrome and for MTS; hence, we propose a broadened clinical criteria for definition of Lynch syndrome that will include sebaceous adenoma, carcinoma, and keratoacanthoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_assertion evidence source_evidence_literature NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_assertion SIO_000772 16826164 NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_assertion wasDerivedFrom befree-20140225 NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_assertion wasGeneratedBy ECO_0000203 NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471508.RAq7-2sF9A5z18NGSSBNzvzy999JAcDeQWSDPqnqB6XVg130_provenance.