Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion type Assertion NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_head.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion description "[Mutations in the PEX1 gene, which encodes a protein of the AAA ATPase family involved in peroxisome matrix protein import, account for the genetic defect in more than half of the patients in this PBD subgroup.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_provenance.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion evidence source_evidence_literature NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_provenance.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion SIO_000772 12402331 NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_provenance.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion wasDerivedFrom befree-20140225 NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_provenance.
- NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_assertion wasGeneratedBy ECO_0000203 NP766271.RAigRkHDaIiPI9HQelSIFegqlaQ1TI2jZGOeO_Sfe_yjg130_provenance.