Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_assertion description "[TNXB, FKBPL and NOTCH4 are all plausible AMD susceptibility genes, but further research will be needed to identify the causal variants and determine whether any of these genes are involved in the pathogenesis of AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_assertion evidence source_evidence_literature NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_assertion SIO_000772 22694956 NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_assertion wasDerivedFrom befree-2016 NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_assertion wasGeneratedBy ECO_0000203 NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.
- befree-2016 importedOn "2016-02-19" NP989785.RARPHUuPASKQrdoNzx6c8q-uM_OjiT_zBCAPMVZ69d_bo130_provenance.