Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion> ?p ?o ?g. }
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- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion type Assertion NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_head.
- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_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." NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_provenance.
- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion evidence source_evidence_literature NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_provenance.
- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion SIO_000772 19680273 NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_provenance.
- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion wasDerivedFrom befree-2016 NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_provenance.
- NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_assertion wasGeneratedBy ECO_0000203 NP757559.RACFUxSNuuQ8mGSfPTEpobkHpmzdYuLV7JgzOekDnIfuQ130_provenance.