Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion> ?p ?o ?g. }
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- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion type Assertion NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_head.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion description "[Mutations in CDH3 gene, encoding P-cadherin, are responsible for hypotrichosis with juvenile macular dystrophy (HJMD), which is a rare autosomal recessive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion evidence source_evidence_literature NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion SIO_000772 20140736 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion wasDerivedFrom befree-20140225 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.
- NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_assertion wasGeneratedBy ECO_0000203 NP929908.RAHxIyaGJHSicsCyM_FXQowWBGyByfypWIvWa4jljxTIU130_provenance.