Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion type Assertion NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_head.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion wasGeneratedBy ECO_0000203 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion wasDerivedFrom befree-2016 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion SIO_000772 16361827 NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion evidence source_evidence_literature NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.
- NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_assertion description "[There are three inheritance patterns of CNDI: the X-linked recessive form associated with vasopressin V2 receptor gene mutations, and the autosomal recessive and dominant forms associated with aquaporin-2 gene (AQP2) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527530.RAtv1ehv3vqNoJVy2YeUB8DM0kKecqZcZ_1vt5rqxf38s130_provenance.