Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion> ?p ?o ?g. }
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- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion type Assertion NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_head.
- 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.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion evidence source_evidence_literature NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion SIO_000772 24570392 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion wasDerivedFrom befree-20150227 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.
- NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_assertion wasGeneratedBy ECO_0000203 NP759230.RAg6DnfmM7kyBJlOy7gnLsJOP3ygSjeR6dzCfqWEp4R_g130_provenance.