Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion> ?p ?o ?g. }
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- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion type Assertion NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_head.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion description "[Of the 97 amino acid substitutions, 11 occurred at a frequency that made them unlikely to be high-penetrance recessive disease-causing variants (HPRDCV). After accounting for variants in cis, one or more changes that were compatible with HPRDCV were found]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion evidence source_evidence_literature NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion SIO_000772 11328725 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion wasDerivedFrom gad-20150221 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.
- NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_assertion wasGeneratedBy ECO_0000203 NP61493.RA5PPgAbt1RAOufWKrjgdZ2t1YwasP5qKYGHRwkb2ctMc130_provenance.