Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion> ?p ?o ?g. }
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- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion type Assertion NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_head.
- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion description "[Fermitin family member 1 (FERMT1, Kindlin-1) is an epithelial-specific regulator of integrin functions and is associated with Kindler syndrome, a genetic disorder characterized by skin blistering, atrophy, and photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_provenance.
- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion evidence source_evidence_literature NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_provenance.
- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion SIO_000772 21832234 NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_provenance.
- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion wasDerivedFrom befree-20150227 NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_provenance.
- NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_assertion wasGeneratedBy ECO_0000203 NP919445.RABDidGlNSnmedFYBq7l5BP54S_UdzkjpEvQ6WgQ0OOjw130_provenance.