Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_assertion description "[AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_assertion evidence source_evidence_curated NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_assertion SIO_000772 16453322 NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_assertion wasDerivedFrom uniprot-20130724 NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_assertion wasGeneratedBy ECO_0000218 NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP263.RAiFWzoab-WcwlwRNNVzypFeno1X6wH2WwrwcCabYkCPA130_provenance.