Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_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." NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_assertion evidence source_evidence_literature NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_assertion SIO_000772 10775052 NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_assertion wasDerivedFrom befree-20140225 NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_assertion wasGeneratedBy ECO_0000203 NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP495473.RAlpg5N0ClX1CUTc61g9DbP2v7x14ExJ29xxnProG2oBw130_provenance.