Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_assertion description "[To describe clinical, pathologic, and genetic features of three FTD patients having either a family history of FTD (A.III.1 and B.II.1) or of ALS (C.III.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_assertion evidence source_evidence_literature NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_assertion SIO_000772 17202431 NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_assertion wasDerivedFrom befree-20140225 NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_assertion wasGeneratedBy ECO_0000203 NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP560336.RAyGfBt2zAZRYjWUg-NwDiBxW2WPYx-9O38IISTQpdpvM130_provenance.