Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- befree-2016 importedOn "2016-02-19" NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_assertion wasGeneratedBy ECO_0000203 NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_assertion wasDerivedFrom befree-2016 NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_assertion SIO_000772 16862116 NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_assertion evidence source_evidence_literature NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.
- NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_assertion description "[Our results identify mutations in PGRN as a cause of neurodegenerative disease and indicate the importance of PGRN function for neuronal survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560957.RA_H5u2I1XqSMW3JeoaYpxpSySA_JI3ZroNk6WyRbTMDM130_provenance.