Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion> ?p ?o ?g. }
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- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion type Assertion NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_head.
- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion description "[As in previously studied patients, adFNDI apparently manifested after birth, was due to a partial or severe deficiency of AVP, and was associated with absence or diminution of the hyperintense MRI signal normally emitted by the posterior pituitary, and with a heterozygous mutation in the AVP-NPII gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_provenance.
- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion evidence source_evidence_literature NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_provenance.
- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion SIO_000772 11980620 NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_provenance.
- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion wasDerivedFrom befree-2016 NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_provenance.
- NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_assertion wasGeneratedBy ECO_0000203 NP353250.RA6yZHTB7iOcajDvtwOE5ig52XRPBxUstp7gyvpuCUJzg130_provenance.