Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion description "[Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion evidence source_evidence_literature NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion SIO_000772 11439091 NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion wasDerivedFrom befree-20140225 NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_assertion wasGeneratedBy ECO_0000203 NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358005.RAiri3Ds7wNZq-P_ehv7WajhzjlP65jG-y65hKlk4Mjs4130_provenance.