Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion description "[TDP-43 positive inclusions are also a feature of amyotrophic lateral sclerosis pathology, corroborating the observation of overlapping clinical features between the two conditions and reaffirming the FTD-ALS disease spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion evidence source_evidence_literature NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion SIO_000772 20413882 NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion wasDerivedFrom befree-20140225 NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_assertion wasGeneratedBy ECO_0000203 NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP184494.RAQnkg-8qzVh7JW77O6_cM19TZRHePhotZysgFZUnzIGs130_provenance.