Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_assertion description "[The most common form of hereditary spastic paraplegia is caused by mutations in the spastin gene (SPG4), which encodes spastin, an adenosine triphosphatase associated with various cellular activities protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_assertion evidence source_evidence_curated NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_assertion SIO_000772 14732620 NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_assertion wasDerivedFrom uniprot-20150221 NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_assertion wasGeneratedBy ECO_0000218 NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4968.RAED5K-crIVakhzO6dFGt52FRN2pR3uQESq7Eogmf-vSE130_provenance.