Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion> ?p ?o ?g. }
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- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion type Assertion NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_head.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion evidence source_evidence_literature NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion SIO_000772 20956273 NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion wasDerivedFrom befree-20140225 NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.
- NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_assertion wasGeneratedBy ECO_0000203 NP363300.RA4JAPspz-q3D_4haAMXCH4_GMBsv1rPQOxGUcF4uKcRk130_provenance.