Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_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." NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_assertion evidence source_evidence_literature NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_assertion SIO_000772 7727782 NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_assertion wasDerivedFrom befree-20150227 NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_assertion wasGeneratedBy ECO_0000203 NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009575.RART0ApFoxg8wQ14vnjaoVBO-Jd-EDqLV-Y4OV3zpg_tk130_provenance.