Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_assertion description "[The P301L mutation is causal for frontotemporal dementia with parkinsonism-17 (FTDP-17), but it has been used for studying memory effects characteristic of AD in transgenic mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_assertion evidence source_evidence_literature NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_assertion SIO_000772 22561128 NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_assertion wasDerivedFrom befree-2016 NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_assertion wasGeneratedBy ECO_0000203 NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.
- befree-2016 importedOn "2016-02-19" NP979876.RAQE7c9cy-O8HIlI3SHhA6DiBKAqLnW20QKqZqsUlxnp4130_provenance.