Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion description "[We tested whether these SNPs are associated with AMD in Israeli populations, if they underlie variable phenotype and response to therapy in neovascular AMD (NVAMD), and if HTRA1 expression in vivo is associated with its promoter variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion evidence source_evidence_literature NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion SIO_000772 19065273 NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion wasDerivedFrom befree-2016 NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion wasGeneratedBy ECO_0000203 NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.
- befree-2016 importedOn "2016-02-19" NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance.