Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion description "[Because not all of our patients harbored mutations in IFT122, CED seems to be genetically heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion evidence source_evidence_curated NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion SIO_000772 20493458 NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion wasDerivedFrom ctd_human-20130708 NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion wasGeneratedBy ECO_0000218 NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_provenance.