Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_assertion description "[The most common first syndrome among the MNDI and DLDH (tau negative) pathologies was FTD-bv, but subsequently progressive aphasia (PA), occasionally CBDS and semantic dementia also developed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_assertion evidence source_evidence_literature NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_assertion SIO_000772 16033782 NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_assertion wasDerivedFrom befree-20140225 NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_assertion wasGeneratedBy ECO_0000203 NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475851.RAElLm_j-ldnVUUNR0s-mTN9pKEWEWeJSQARcsVhsQMC8130_provenance.