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- source_evidence_literature type ECO_0000212 NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_assertion description "[Based on in-silico analysis, a case-control study including 420 HCC patients and 420 healthy controls was conducted to investigate the association between HCC susceptibility with a 4-bp insertion/deletion polymorphism (rs17875871) in the 3'UTR of IFNAR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_assertion evidence source_evidence_literature NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_assertion SIO_000772 22824466 NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_assertion wasDerivedFrom befree-20140225 NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_assertion wasGeneratedBy ECO_0000203 NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP473939.RAKoktT4Hs5VwXsV7lYPFW1_9cOo_i7QDWV8AHW0jTtYo130_provenance.