Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_assertion description "[Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: motor neuron disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_assertion evidence source_evidence_literature NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_assertion SIO_000772 7166018 NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_assertion wasDerivedFrom befree-20140225 NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_assertion wasGeneratedBy ECO_0000203 NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP603064.RAdeNHFhba0MsjSE_1UuSllgH7ACBuyV8jOQwDMrNLpLk130_provenance.