Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_assertion description "[Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_assertion evidence source_evidence_literature NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_assertion SIO_000772 20111867 NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_assertion wasDerivedFrom befree-2016 NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_assertion wasGeneratedBy ECO_0000203 NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.
- befree-2016 importedOn "2016-02-19" NP790312.RAQx3wbtpz7fsIymonHtdXJntyHY_TMMMYFFIsixmL7z0130_provenance.