Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion> ?p ?o ?g. }
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- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion type Assertion NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_head.
- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion description "[This paper reports the clinical and metabolic findings in two sibling sisters born with fetal hydrops and eventually found to have deficient S-adenosylhomocysteine hydrolase (AHCY) activity due to compound heterozygosity for two novel mutations, c.145C>T; p.Arg49Cys and c.257A>G; p.Asp86Gly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_provenance.
- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion evidence source_evidence_literature NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_provenance.
- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion SIO_000772 20852937 NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_provenance.
- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion wasDerivedFrom befree-20150227 NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_provenance.
- NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_assertion wasGeneratedBy ECO_0000203 NP231213.RAtNVpSjrlny_Js9HXoxCvcS9jvO_1R_tAS-3YPNgcSog130_provenance.