Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion> ?p ?o ?g. }
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- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion type Assertion NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_head.
- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion description "[Consequently, 86% of afibrinogenemia alleles analyzed to date have truncating mutations of FGA, though mutations in all 3 fibrinogen genes, FGG, FGA, and FGB, might be predicted to cause congenital afibrinogenemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_provenance.
- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion evidence source_evidence_curated NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_provenance.
- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion SIO_000772 10891444 NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_provenance.
- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion wasDerivedFrom ctd_human-20150221 NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_provenance.
- NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_assertion wasGeneratedBy ECO_0000218 NP14589.RARl_w9N1VCJp_9FYpxQqvtIpZo4LPX1LjKfGRmP5maBQ130_provenance.