Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion> ?p ?o ?g. }
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- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion type Assertion NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_head.
- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion description "[Dominant mutations in the receptor calcium channel gene TRPV4 have been associated with a family of skeletal dysplasias (metatropic dysplasia, pseudo-Morquio type 2, spondylometaphyseal dysplasia, Kozlowski type, brachyolmia, and familial digital arthropathy) as well as with dominantly inherited neuropathies (hereditary motor and sensory neuropathy 2C, scapuloperoneal spinal muscular atrophy, and congenital distal spinal muscular atrophy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_provenance.
- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion evidence source_evidence_literature NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_provenance.
- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion SIO_000772 21964829 NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_provenance.
- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion wasDerivedFrom befree-20140225 NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_provenance.
- NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_assertion wasGeneratedBy ECO_0000203 NP808691.RAOLJTC9tL_ppL5hCwoBV27bsKMDMiDmNRcXmEVFiZ2xU130_provenance.