Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion type Assertion NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_head.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion wasGeneratedBy ECO_0000203 NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_provenance.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion wasDerivedFrom befree-2016 NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_provenance.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion SIO_000772 19068082 NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_provenance.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion evidence source_evidence_literature NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_provenance.
- NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_assertion description "[Neither mutation hot spot nor phenotype–genotype correlation has been established in MEN1 although some missense mutations may be specifically associated with a phenotype of familial isolated hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708153.RAa1Uw0pWS0VaHdSsHeEaUWasE70V9yR2ECMKE3WxXFAo130_provenance.