Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion> ?p ?o ?g. }
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- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion type Assertion NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_head.
- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion description "[Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion evidence source_evidence_literature NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion SIO_000772 20686492 NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion wasDerivedFrom befree-20140225 NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_assertion wasGeneratedBy ECO_0000203 NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.