Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion type Assertion NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_head.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion description "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion evidence source_evidence_literature NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion SIO_000772 9690138 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion wasDerivedFrom befree-20140225 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion wasGeneratedBy ECO_0000203 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.