Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion> ?p ?o ?g. }
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- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion type Assertion NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_head.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion description "[Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion evidence source_evidence_curated NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion SIO_000772 22544363 NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion wasDerivedFrom ctd_human-2016 NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.
- NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_assertion wasGeneratedBy ECO_0000218 NP31279.RAgEf2kduWrXKz5301ZLmHBClitI8Lysl9uo8HCgvbYnQ130_provenance.