Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion> ?p ?o ?g. }
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- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion type Assertion NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_head.
- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion wasGeneratedBy ECO_0000203 NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_provenance.
- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion wasDerivedFrom befree-20140225 NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_provenance.
- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion SIO_000772 22578324 NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_provenance.
- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion evidence source_evidence_literature NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_provenance.
- NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_assertion description "[Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurodevelopmental disorders with contrasting anxiety phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910877.RAmff9rfjQanb4x401-lHZkH6Xlxvd8_Qk7To9j0VUHps130_provenance.