Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- befree-2016 importedOn "2016-02-19" NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_assertion wasGeneratedBy ECO_0000203 NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_assertion wasDerivedFrom befree-2016 NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_assertion SIO_000772 17828778 NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_assertion evidence source_evidence_literature NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.
- NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_assertion description "[In patients with extensive UC a significantly different distribution of genotypes of the MDR1 G/A change located in intron 3 (rs3789243) was observed between carriers/noncarriers of the -25385T risk allele (P = 0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629257.RAqWKoN6ryqFJTCAp1AfSrWwwTX2P1MkE8VIP8ETL0ANM130_provenance.