Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion> ?p ?o ?g. }
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- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion type Assertion NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_head.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion wasGeneratedBy ECO_0000203 NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion wasDerivedFrom befree-20140225 NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion SIO_000772 23335808 NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion evidence source_evidence_literature NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_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." NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.