Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion> ?p ?o ?g. }
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- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion type Assertion NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_head.
- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion description "[BOR syndrome is an autosomal dominant trait encompassing branchial, otic and renal anomalies because of mutations in EYA1, SIX1 and SIX5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_provenance.
- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion evidence source_evidence_literature NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_provenance.
- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion SIO_000772 18177466 NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_provenance.
- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion wasDerivedFrom befree-2016 NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_provenance.
- NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_assertion wasGeneratedBy ECO_0000203 NP648507.RAigFJuL2CtkHTJXhUvzdSyzVYqjl4ehL_xnhqJcuMIYI130_provenance.