Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_assertion description "[The index case and his mother had both SCA2 and SCA10 mutations with a combined clinical phenotype of both disorders, including slow saccades (SCA2) and seizures (SCA10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_assertion evidence source_evidence_literature NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_assertion SIO_000772 25630585 NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_assertion wasDerivedFrom befree-2016 NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_assertion wasGeneratedBy ECO_0000203 NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259140.RAtTpgAUJD2eOLFFu9yvSlIErf6vODmUHDRZYRgGX27rI130_provenance.