Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_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." NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_assertion evidence source_evidence_curated NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_assertion SIO_000772 11439091 NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_assertion wasDerivedFrom uniprot-20130724 NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_assertion wasGeneratedBy ECO_0000218 NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4883.RA1yfX_2fNmnIu3BY8kJSQ0gm9rEKkGfomN7TxJoH3PCs130_provenance.