Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_assertion description "[K-ras point mutations were observed in 1/2 of the atypical hyperplasia (codon 12: GGT-->GTT) and 3/9 of the carcinoma (codon 12: GGT-->GAT, GGT-->AGT, codon 61: CAA-->CAC), while they were not detected in 7 of the normal tissues and in 5 of the simple or complex hyperplasia without atypia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_assertion evidence source_evidence_literature NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_assertion SIO_000772 10775052 NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_assertion wasDerivedFrom befree-20150227 NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_assertion wasGeneratedBy ECO_0000203 NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1005583.RAaIRvPD0pqGOnA6E2gp21OAZUG8x91pMCXXDOTnGENfA130_provenance.