Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion> ?p ?o ?g. }
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- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion type Assertion NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_head.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion wasGeneratedBy ECO_0000203 NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion wasDerivedFrom befree-20140225 NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion SIO_000772 23335808 NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion evidence source_evidence_literature NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_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." NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.