Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_assertion description "[The other mutation detected in MLH1 was a TAC-->TAA substitution codon 750 (exon 19) creating a stop codon, predicted to generate a truncated protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_assertion evidence source_evidence_literature NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_assertion SIO_000772 11369138 NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_assertion wasDerivedFrom befree-20140225 NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_assertion wasGeneratedBy ECO_0000203 NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP246396.RAGR1brUKXQtO8lScaujRhJVZMOL7-gQai_s19VGQ7vAI130_provenance.