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- source_evidence_literature type ECO_0000212 NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_assertion description "[By sequencing candidate genes, we identified recessive LRP4 mutations in 12 families with CLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_assertion evidence source_evidence_literature NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_assertion SIO_000772 20381006 NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_assertion wasDerivedFrom befree-20140225 NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_assertion wasGeneratedBy ECO_0000203 NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP235674.RAfOj6OnFqNERgS5c-9-p_5M0UZ_Re-T15tVlHqNZZOlQ130_provenance.