Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion> ?p ?o ?g. }
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- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion type Assertion NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_head.
- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion description "[Our studies suggest that mutations in PDGFRB are a cause of IM and highlight NOTCH3 as a candidate gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.
- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion evidence source_evidence_literature NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.
- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion SIO_000772 23731542 NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.
- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion wasDerivedFrom befree-20140225 NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.
- NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_assertion wasGeneratedBy ECO_0000203 NP177793.RA7564V9x0Xq0o8yX0ieklnhW4FYc3rFYQXzGqQEYmj3I130_provenance.