Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_assertion description "[67 unrelated cystic fibrosis (CF) patients were screened for some of the most common mutations of the CFTR gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_assertion evidence source_evidence_literature NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_assertion SIO_000772 7542223 NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_assertion wasDerivedFrom befree-2016 NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_assertion wasGeneratedBy ECO_0000203 NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311671.RAGDDV8miwHQGnENaQkH8q9IL5p2WWVgTm6lA0qcmid9o130_provenance.