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- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion type Assertion NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_head.
- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion description "[Ardalan-Shoja-Kiuru syndrome, a hereditary gelsolin amyloidosis plus retinitis pigmentosa, is due to a G654A gelsolin mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_provenance.
- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion evidence source_evidence_literature NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_provenance.
- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion SIO_000772 17720986 NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_provenance.
- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion wasDerivedFrom lhgdn-20090331 NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_provenance.
- NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_assertion wasGeneratedBy ECO_0000203 NP228558.RANs3xfkm2Cjyq1GZ3g3A4WFHK3CdGHndEcYQJpHC-S9A130_provenance.