Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion> ?p ?o ?g. }
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- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion type Assertion NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_head.
- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_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." NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_provenance.
- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion evidence source_evidence_literature NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_provenance.
- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion SIO_000772 20818383 NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_provenance.
- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion wasDerivedFrom befree-20150227 NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_provenance.
- NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_assertion wasGeneratedBy ECO_0000203 NP948527.RAaTcmYH2PjMYvsoigF_cztXHX0UK2rmNOkw4xcpzVGdg130_provenance.