Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion> ?p ?o ?g. }
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- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion type Assertion NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_head.
- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.
- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion evidence source_evidence_literature NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.
- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion SIO_000772 12445216 NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.
- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion wasDerivedFrom befree-20140225 NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.
- NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_assertion wasGeneratedBy ECO_0000203 NP667759.RA1g1Q0FY8ZKcVASEqjVFicH2e-WMVd5-saaovoi8iSuc130_provenance.