Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion type Assertion NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_head.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion description "[Mutations in TRPV4, encoding a cation channel, have recently been identified in one large dominant congenital spinal muscular atrophy kindred, but the genetic basis of dominant congenital spinal muscular atrophy in many families remains unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_provenance.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion evidence source_evidence_literature NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_provenance.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion SIO_000772 22628388 NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_provenance.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion wasDerivedFrom befree-20150227 NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_provenance.
- NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_assertion wasGeneratedBy ECO_0000203 NP935098.RAm6e4eNKBsAP1AP6RST4NIl1Qz3ksOH68FchRqr9V718130_provenance.