Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP835031.RAL6XZDCQIHjkQNFIvPWHj2M8_FP5hfdWT1F23xK64Izg130_provenance.