Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_assertion description "[Further analyses of DHFR, MLL, MYC, and RFC gene status in four additional human OS cell lines revealed that only gain of DHFR and MLL were associated with an inherent lower sensitivity to MTX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_assertion evidence source_evidence_literature NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_assertion SIO_000772 14582536 NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_assertion wasDerivedFrom befree-2016 NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_assertion wasGeneratedBy ECO_0000203 NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.
- befree-2016 importedOn "2016-02-19" NP418489.RAnDI28AsNxXfiWXXlV7oNhb0dK6OruBtf1_wg_Rme-w4130_provenance.