Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_assertion description "[This R1810me2s modification requires protein arginine methyltransferase 5 (PRMT5) and recruits the Tudor domain of the survival of motor neuron (SMN, also known as GEMIN1) protein, which is mutated in spinal muscular atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_assertion evidence source_evidence_literature NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_assertion SIO_000772 26700805 NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_assertion wasDerivedFrom befree-2016 NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_assertion wasGeneratedBy ECO_0000203 NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295828.RA00AqFjGTwb9WRLQ88NGYXKoPHnmLmXAf4r_P-motDv0130_provenance.