Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion> ?p ?o ?g. }
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- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion type Assertion NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_head.
- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion description "[Suspected microdeletion syndromes such as deletion 22q11.2, Williams-Beuren and Angelman syndromes were excluded before array-CGH analysis was performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_provenance.
- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion evidence source_evidence_literature NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_provenance.
- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion SIO_000772 17901693 NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_provenance.
- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion wasDerivedFrom befree-2016 NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_provenance.
- NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_assertion wasGeneratedBy ECO_0000203 NP632352.RA6rB3F1mn69QNj6yR4OFYMzPoSeHvgdyYJ1zt8WjPVDM130_provenance.