Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion type Assertion NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_head.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion description "[The hypocalciuric, hypomagnesemic variant of Bartter syndrome (Gitelman syndrome), presents in early adulthood with predominantly musculoskeletal symptoms and is due to mutations in the gene encoding the Na-Cl cotransporter (NCCT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion evidence source_evidence_literature NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion SIO_000772 11780689 NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion wasDerivedFrom befree-2016 NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.
- NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_assertion wasGeneratedBy ECO_0000203 NP341299.RA4grIW2Yhcu_BsSXFqdANa_pRF4F5ZcfF1RdetJSVmho130_provenance.