Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_assertion wasGeneratedBy ECO_0000203 NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_assertion wasDerivedFrom befree-20140225 NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_assertion SIO_000772 20533283 NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_assertion evidence source_evidence_literature NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_assertion description "[We verified that the frequency of MSI was similar in familial and sporadic GC settings, demonstrating that this molecular phenotype is not a hallmark of familial GC in contrast to what is verified in HNPCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP422000.RArk5EBWm3I_z8AqjilTLjB8wn4KbxYZGtsTm88mR6EIA130_provenance.