Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion> ?p ?o ?g. }
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- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion type Assertion NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_head.
- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion description "[We report that hypofunctional alleles of WNT1 cause autosomal-recessive osteogenesis imperfecta, a congenital disorder characterized by reduced bone mass and recurrent fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_provenance.
- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion evidence source_evidence_literature NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_provenance.
- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion SIO_000772 23499309 NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_provenance.
- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion wasDerivedFrom befree-20140225 NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_provenance.
- NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_assertion wasGeneratedBy ECO_0000203 NP684142.RAJXvAUinW3sosyAbDZGf1v3pNKLaBXMvsXL30VwPtFWg130_provenance.