Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- befree-2016 importedOn "2016-02-19" NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_assertion wasGeneratedBy ECO_0000203 NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_assertion wasDerivedFrom befree-2016 NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_assertion SIO_000772 17715352 NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_assertion evidence source_evidence_literature NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.
- NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_assertion description "[TAU gene mutations that alter the inclusion of exon 10, and hence the 4R:3R ratio, are causal in the tauopathy frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626373.RAHjdfh5y9XUvHcHKzlJNi3hqnb0Sk1tM6weWLgUR_o-c130_provenance.