Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion wasGeneratedBy ECO_0000203 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion wasDerivedFrom befree-20150227 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion SIO_000772 24570392 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion evidence source_evidence_literature NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion description "[LAM occurs sporadically or in patients with tuberous sclerosis complex (TSC) and is etiologically linked to mutations in the TSC1 and TSC2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.