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- source_evidence_literature type ECO_0000212 NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_assertion description "[Frequencies and distributions of NAT2 and UGT1A7 SNPs as well as their haplotypes were investigated in 95 patients with UC, 60 patients with CD, and 200 gender-matched, unrelated, healthy, control volunteers by PCR-restriction fragment length polymorphism (RFLP), PCR-denaturing high-performance liquid chromatography (DHPLC), and direct DNA sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_assertion evidence source_evidence_literature NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_assertion SIO_000772 16097053 NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_assertion wasDerivedFrom befree-20140225 NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_assertion wasGeneratedBy ECO_0000203 NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP440629.RAA65fMxK-cd46MfvNqxqoLa4uEhmDlKlBRJFQ0Jlw8xk130_provenance.