Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion> ?p ?o ?g. }
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- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion type Assertion NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_head.
- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion wasGeneratedBy ECO_0000218 NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_provenance.
- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion wasDerivedFrom uniprot-2016 NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_provenance.
- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion SIO_000772 8045958 NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_provenance.
- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion evidence source_evidence_curated NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_provenance.
- NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_assertion description "[A de novo mutation in the coding sequence for neurophysin-II (Pro24-->Leu) is associated with onset and transmission of autosomal dominant neurohypophyseal diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8706.RAA6L-C9gjwTv_a9DiNDuSUyCP3XHiHUAEjOYOebqeDG8130_provenance.