Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_assertion description "[UBB+1, a mutant form of ubiquitin was present in the majority of NFTs, whereas co-existence of alpha-synuclein and UBB+1 was found in only a few neurons in cases of combined multiple system atrophy and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_assertion evidence source_evidence_literature NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_assertion SIO_000772 17237936 NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_assertion wasDerivedFrom lhgdn-20090331 NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_assertion wasGeneratedBy ECO_0000203 NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP110978.RALVoU8KDK3n39EQEW97Ja0n2JzsN4EJDtUrOKTeIo80w130_provenance.