Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion description "[It confirms PHOX2A as the autosomal recessive CFEOM2 disease gene and provides evidence that the phenotypic differences between PHOX2A mutations in man and mouse do not result from hypomorphic PHOX2A alleles in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion evidence source_evidence_literature NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion SIO_000772 14597037 NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion wasDerivedFrom befree-20140225 NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_assertion wasGeneratedBy ECO_0000203 NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP843560.RAt_KU-zzyqiFPOZUc8ZpC6YN-R2JFyjZtp9qoM1eHs5A130_provenance.