Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion> ?p ?o ?g. }
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- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion type Assertion NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_head.
- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion description "[ PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined. Our data may facilitate future investigations of patients with various (other) forms of inherited retinal ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance.
- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion evidence source_evidence_literature NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance.
- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion SIO_000772 16288196 NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance.
- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion wasDerivedFrom gad-20150221 NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance.
- NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion wasGeneratedBy ECO_0000203 NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance.