Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_assertion description "[For example, misfolding of insulin can result in autosomal dominant mutant INS gene-induced diabetes of youth, and misfolding of thyroglobulin can result in autosomal recessive congenital hypothyroidism with deficient thyroglobulin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_assertion evidence source_evidence_literature NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_assertion SIO_000772 23722904 NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_assertion wasDerivedFrom befree-2016 NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_assertion wasGeneratedBy ECO_0000203 NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1082102.RAEcg93PyWVbWt8V6BhgvX7Q_XBrx5LZ-BtTbsUlsm62c130_provenance.