Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_assertion description "[Mutations that cause X-linked agammaglobulinemia (XLA) appear throughout the Bruton tyrosine kinase (Btk) sequence, including the pleckstrin homology (PH) domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_assertion evidence source_evidence_literature NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_assertion SIO_000772 15082835 NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_assertion wasDerivedFrom befree-2016 NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_assertion wasGeneratedBy ECO_0000203 NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.
- befree-2016 importedOn "2016-02-19" NP439710.RA8QXNXjR6c-kElEWBekWmkuEMzNpuLfV8DGM1IXneBKI130_provenance.