Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion type Assertion NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_head.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion wasGeneratedBy ECO_0000203 NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion wasDerivedFrom befree-20150227 NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion SIO_000772 23335808 NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion evidence source_evidence_literature NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_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." NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.