Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_assertion description "[The SERPING1 gene is comprehensively investigated in this study (using three tSNPs), and its genetic variants are evaluated in the largest neovascular AMD cohort to date. The hypothesis that SERPING1 has a modest effect on the risk of neovascular AMD is s]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_assertion evidence source_evidence_literature NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_assertion SIO_000772 20606025 NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_assertion wasDerivedFrom gad-20150221 NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_assertion wasGeneratedBy ECO_0000203 NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180659.RAPHyQyUR2uyQ6n2r4HUyONM0xIrUU7MTwTxNNfovQdRk130_provenance.