Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_assertion wasGeneratedBy ECO_0000218 NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_assertion wasDerivedFrom uniprot-20130724 NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_assertion SIO_000772 20818383 NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_assertion evidence source_evidence_curated NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_assertion description "[High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4221.RAShbq2LD4xYah5JlYc5pF4z5z6_BzWlE0UHP7ur9GT0g130_provenance.