Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_assertion description "[Highly myopic elderly Japanese patients with and without CNV were genotyped for three AMD-associated single nucleotide polymorphisms (SNPs), namely rs10490924 (A69S) of ARMS2, rs11200638 of HTRA1, and rs1061170 (Y402H) of complement factor H (CFH), with the TaqMan SNP assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_assertion evidence source_evidence_literature NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_assertion SIO_000772 19680273 NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_assertion wasDerivedFrom befree-2016 NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_assertion wasGeneratedBy ECO_0000203 NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.
- befree-2016 importedOn "2016-02-19" NP757557.RAPBu0WbQOYBpvimVSPFZjySmkn35g3WgJFQSuXWGVOFk130_provenance.