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- source_evidence_literature type ECO_0000212 NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_assertion description "[We found only one mutation of the N-ras gene that was a 2-bp substitution of GGT(Gly) to GTC(Val) at codon 13 among 22 t(1;19)-ALL cases and five cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_assertion evidence source_evidence_literature NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_assertion SIO_000772 7727782 NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_assertion wasDerivedFrom befree-20140225 NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_assertion wasGeneratedBy ECO_0000203 NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP796097.RASqm5jf2-GKOlX9GG96aV0ST6oY7WTk_bZ4fng6-DR3o130_provenance.