Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion> ?p ?o ?g. }
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- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion type Assertion NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_head.
- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_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." NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_provenance.
- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion evidence source_evidence_literature NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_provenance.
- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion SIO_000772 17720986 NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_provenance.
- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion wasDerivedFrom lhgdn-20090331 NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_provenance.
- NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_assertion wasGeneratedBy ECO_0000203 NP228559.RAafmyTcSADnAg1B2o2YIQfYhrS4ThTIH-o3V-L_EtURw130_provenance.