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- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion type Assertion NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_head.
- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion wasGeneratedBy ECO_0000218 NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_provenance.
- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion wasDerivedFrom uniprot-2016 NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_provenance.
- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion SIO_000772 15863660 NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_provenance.
- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion evidence source_evidence_curated NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_provenance.
- NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_assertion description "[Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4019.RAK39ENEOzs9Fu6g0bH6RctsDCcHYx33XcmHlbtO6NfDY130_provenance.