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- source_evidence_literature type ECO_0000212 NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_assertion description "[Here we consider how knowledge of the impact of PDB-associated SQSTM1 mutations (several of which are now known to be relevant for ALS/FTLD) on these pathways, as well as the locations of the mutations within the p62 primary sequence, may provide new insights into ALS/FTLD disease mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_assertion evidence source_evidence_literature NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_assertion SIO_000772 24486447 NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_assertion wasDerivedFrom befree-2016 NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_assertion wasGeneratedBy ECO_0000203 NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1151072.RAulpOHMVYduGq31CCuJPnaPtUUhCtDeM8oaeRv97BNvU130_provenance.