Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion> ?p ?o ?g. }
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- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion type Assertion NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_head.
- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion description "[CDPX2 patients display skin defects including linear or whorled atrophic and pigmentary lesions, striated hyperkeratosis, coarse lusterless hair and alopecia, cataracts and skeletal abnormalities including short stature, rhizomelic shortening of the limbs, epiphyseal stippling and craniofacial defects (MIM 302960).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_provenance.
- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion evidence source_evidence_literature NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_provenance.
- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion SIO_000772 10391218 NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_provenance.
- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion wasDerivedFrom befree-20140225 NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_provenance.
- NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_assertion wasGeneratedBy ECO_0000203 NP886403.RAmoKGWKmOcbFJ8R0EVJ6OnNJd6vRzZAtEUnVyvYXUZIQ130_provenance.