Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion> ?p ?o ?g. }
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- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion type Assertion NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_head.
- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion description "[We identified three girls with classical CFNS and mild developmental delay harboring de novo deletions of the EFNB1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_provenance.
- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion evidence source_evidence_literature NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_provenance.
- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion SIO_000772 17941886 NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_provenance.
- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion wasDerivedFrom befree-20140225 NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_provenance.
- NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_assertion wasGeneratedBy ECO_0000203 NP674874.RAGZdQ8OoxoQAgBK3xOoN-l24qLkmYgw1MZWl29QFWbqA130_provenance.