Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_assertion description "[Our results indicate that in the Japanese, as has been seen elsewhere, abnormality of the DCX gene is the common cause of SCLH and ILS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_assertion evidence source_evidence_literature NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_assertion SIO_000772 10807542 NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_assertion wasDerivedFrom befree-2016 NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_assertion wasGeneratedBy ECO_0000203 NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.
- befree-2016 importedOn "2016-02-19" NP283593.RAA2gggtiZ_HEb2lakZeKO-OG_ndnqBv86m_SAf2Z5X2o130_provenance.