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- source_evidence_literature type ECO_0000212 NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_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." NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_assertion evidence source_evidence_literature NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_assertion SIO_000772 24486447 NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_assertion wasDerivedFrom befree-20150227 NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_assertion wasGeneratedBy ECO_0000203 NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP902676.RAuJT04CK-kH9q5Ra2Wsyl0Ln7k0S03bJAuPXKCBVHK9c130_provenance.