Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_assertion description "[On the other hand, the common BSEP polymorphism V444A (c.1331T>C; allele frequency 65%) emerged as an independent predictor of the success rate in patients with chronic hepatitis C treated with pegylated interferon/ribavirin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_assertion evidence source_evidence_literature NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_assertion SIO_000772 21691112 NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_assertion wasDerivedFrom befree-2016 NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_assertion wasGeneratedBy ECO_0000203 NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.
- befree-2016 importedOn "2016-02-19" NP903635.RAwYGvTddcc0ufanT9hhQypm7LWTN7975lFPcyWVFGCzA130_provenance.