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- source_evidence_literature type ECO_0000212 NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_assertion description "[Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_assertion evidence source_evidence_literature NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_assertion SIO_000772 15336687 NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_assertion wasDerivedFrom befree-2016 NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_assertion wasGeneratedBy ECO_0000203 NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.
- befree-2016 importedOn "2016-02-19" NP457855.RAtgRYhASor0dqJ0SikojS94_kwo3PYbDxSq3H5seE5vk130_provenance.