Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion> ?p ?o ?g. }
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- NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_assertion type Assertion NP19230.RAD6xI7ru2UmBqbXAl2SSgftO45YZ7_3MYLq1weITvJKA130_head.
- 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.