Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion> ?p ?o ?g. }
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- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion type Assertion NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_head.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion wasGeneratedBy ECO_0000203 NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion wasDerivedFrom befree-20150227 NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion SIO_000772 23335808 NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion evidence source_evidence_literature NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.