Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion> ?p ?o ?g. }
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- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion type Assertion NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_head.
- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_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." NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_provenance.
- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion evidence source_evidence_curated NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_provenance.
- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion SIO_000772 20818383 NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_provenance.
- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion wasDerivedFrom ctd_human-20130708 NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_provenance.
- NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_assertion wasGeneratedBy ECO_0000218 NP16161.RA-qsgP6pScA3eeX84iS0Js_hdC6DSfO6cLRJUb4MnXs0130_provenance.