Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_assertion description "[Among 34 tissues specimens surgically resected from 30 patients and 5 cell lines of human HCC, only two had ras point mutations; in one case, codon 12 of c-Ki-ras was altered from GGT, coding glycine, to GTT, coding valine; in the other case, codon 61 of N-ras was altered from CAA, coding glutamine, to AAA, coding lysine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_assertion evidence source_evidence_literature NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_assertion SIO_000772 2542205 NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_assertion wasDerivedFrom befree-20140225 NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_assertion wasGeneratedBy ECO_0000203 NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP289631.RAF5sHGq1nNlbE0gmLs4murLHXeeSQlMHBRLaXsk4l2uk130_provenance.