Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_assertion description "[Copy number variations in regulators of complement activation genes (CFHR1 and CFHR3) and glutathione S transferase genes (GSTM1 and GSTT1) have been associated with AMD, and several additional loci have been identified as regions of potential interest but require further evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_assertion evidence source_evidence_literature NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_assertion SIO_000772 23244519 NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_assertion wasDerivedFrom befree-2016 NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_assertion wasGeneratedBy ECO_0000203 NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1036646.RAJJ9a0KLkpdUD8wFKpPOUVXhk4wP07g2ZoURNJEdoh5k130_provenance.