Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion type Assertion NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_head.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion wasGeneratedBy ECO_0000203 NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_provenance.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion wasDerivedFrom gad-20150221 NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_provenance.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion SIO_000772 12853230 NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_provenance.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion evidence source_evidence_literature NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_provenance.
- NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_assertion description "[We conclude that SCA-17 repeat expansion mutations are not a common cause of familial parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63098.RAVsMQrwTJ25d7-UcoTHB-W-pMyg-VXahRPPfF3p-aCo4130_provenance.