Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion> ?p ?o ?g. }
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- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion type Assertion NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_head.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion description "[PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion evidence source_evidence_literature NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion SIO_000772 16288196 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion wasDerivedFrom befree-20150227 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.
- NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_assertion wasGeneratedBy ECO_0000203 NP961716.RAaAYMg5S7NyHM7XaCllapdZj4aibzD1k6miNE7GalHPk130_provenance.