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- source_evidence_literature type ECO_0000212 NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_assertion description "[We genotyped patients with diagnosis of MCS, suspected MCS and Italian healthy controls for allelic variants of cytochrome P450 isoforms (CYP2C9, CYP2C19, CYP2D6, and CYP3A5), UDP-glucuronosyl transferase (UGT1A1), and glutathione S-transferases (GSTP1, GSTM1, and GSTT1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_assertion evidence source_evidence_literature NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_assertion SIO_000772 20430047 NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_assertion wasDerivedFrom gad-20150221 NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_assertion wasGeneratedBy ECO_0000203 NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137597.RA_Rlhk-7DzkQHSmLMF6vmgBChPN5hnCzVyCh82Gpl5bE130_provenance.