Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_assertion description "[Spastic paraplegia type 2 (SPG2) is allelic to Pelizaeus-Merzbacher disease (PMD), with both conditions resulting from mutations in the proteolipid protein gene (PLP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_assertion evidence source_evidence_curated NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_assertion SIO_000772 10319897 NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_assertion wasDerivedFrom uniprot-2016 NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_assertion wasGeneratedBy ECO_0000218 NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP171.RAq-zEiOaj-VhMKbPJX8dOEGuvg7aEvApW0QD4HTKUGyA130_provenance.