Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_assertion description "[Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_assertion evidence source_evidence_curated NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_assertion SIO_000772 19508969 NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_assertion wasDerivedFrom ctd_human-2016 NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_assertion wasGeneratedBy ECO_0000218 NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP24223.RAZQAom0iojz6P9-UczByDe9Zu_aMaBFXPOTEyNfhgBng130_provenance.