Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion evidence source_evidence_curated NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion SIO_000772 20493458 NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion wasDerivedFrom ctd_human-2016 NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_assertion wasGeneratedBy ECO_0000218 NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP26210.RAQASYcBW5uym1tuWLIVMpt0SJFgmo0_su75G2QnBwu8Q130_provenance.