Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion> ?p ?o ?g. }
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- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion type Assertion NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_head.
- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion description "[Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_provenance.
- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion evidence source_evidence_literature NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_provenance.
- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion SIO_000772 16244783 NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_provenance.
- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion wasDerivedFrom befree-2016 NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_provenance.
- NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_assertion wasGeneratedBy ECO_0000203 NP519198.RACsfzGkOS7Il4HzL-leYBJxQOFaha8fUIeg05bGrcj0o130_provenance.