Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_assertion description "[Phosphorylated TDP-43 also accumulates in the detergent-insoluble fraction from affected brain regions of Gfap(R236H/+) knock-in mice, which harbor a GFAP mutation homologous to one that causes AxD in humans, and TDP-43 colocalizes with astrocytic RF pathology in Gfap(R236H/+) mice and transgenic mice overexpressing human wild-type GFAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_assertion evidence source_evidence_literature NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_assertion SIO_000772 24806671 NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_assertion wasDerivedFrom befree-2016 NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_assertion wasGeneratedBy ECO_0000203 NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1180369.RAwvPes421wGYJ-RcXjzotkUd8QDLUWD_MXb6VExBe9dA130_provenance.