Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- befree-2016 importedOn "2016-02-19" NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_assertion wasGeneratedBy ECO_0000203 NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_assertion wasDerivedFrom befree-2016 NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_assertion SIO_000772 18782298 NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_assertion evidence source_evidence_literature NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.
- NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_assertion description "[Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692318.RAPxrvssKlPsIbVgUuZPmaAeO3OUlRiK7IlC_e5b8Nm6U130_provenance.