Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_assertion description "[AFG3L2 forms either a homo-oligomeric isoenzyme or a hetero-oligomeric complex with paraplegin, a homologous protein mutated in hereditary spastic paraplegia type 7 (SPG7).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_assertion evidence source_evidence_literature NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_assertion SIO_000772 22022284 NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_assertion wasDerivedFrom befree-20150227 NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_assertion wasGeneratedBy ECO_0000203 NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710216.RAn5pttLY_uhGj6gByK1jz8A91uhSvv8L2xYAYRQIaikE130_provenance.