Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion type Assertion NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_head.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion description "[DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_provenance.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion evidence source_evidence_literature NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_provenance.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion SIO_000772 2896160 NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_provenance.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion wasDerivedFrom befree-20140225 NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_provenance.
- NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_assertion wasGeneratedBy ECO_0000203 NP181351.RAtIO8Bmiyh7pDcatImLkCViVd7dj9CHN6RL6MNCelrX4130_provenance.