Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_assertion description "[No evidence for association of advanced AMD with other previous reported susceptibility genes, such as CST3, CX3CR1, FBLN5, HMCN1, PON1, SOD2, TLR4, VEGF and VLDLR, was detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_assertion evidence source_evidence_literature NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_assertion SIO_000772 21106043 NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_assertion wasDerivedFrom befree-20140225 NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_assertion wasGeneratedBy ECO_0000203 NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP879395.RAKDilhXkQHt0nvq0yZuNarNK2Nk0gTvR0ATUnvdCys2E130_provenance.