Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion> ?p ?o ?g. }
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- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion type Assertion NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_head.
- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion description "[We searched for mutations in the KRT5 gene, a causative gene for the similar pigmentation disorder Dowling-Degos disease (DDD), in all the patients and found no KRT5 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_provenance.
- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion evidence source_evidence_literature NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_provenance.
- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion SIO_000772 23666529 NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_provenance.
- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion wasDerivedFrom befree-20140225 NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_provenance.
- NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_assertion wasGeneratedBy ECO_0000203 NP662976.RAmYCJ4Gt4LMsE8pqb7ZcUq5wJVcpYSzvoAspxQeDOwcM130_provenance.