Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_assertion description "[The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_assertion evidence source_evidence_literature NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_assertion SIO_000772 15138899 NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_assertion wasDerivedFrom befree-20140225 NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_assertion wasGeneratedBy ECO_0000203 NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP503363.RAeD_jlB7AFZfLToyP7mQgpcnQ5CBp0rKljUd-4sWhtQY130_provenance.