Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion> ?p ?o ?g. }
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- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion type Assertion NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_head.
- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion wasGeneratedBy ECO_0000203 NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_provenance.
- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion wasDerivedFrom befree-20140225 NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_provenance.
- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion SIO_000772 20357205 NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_provenance.
- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion evidence source_evidence_literature NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_provenance.
- NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_assertion description "[Common mutations for Leber's hereditary optic neuropathy (LHON: G11778A; T14484C; and G3460A) were not present in AMD samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460170.RAEr_xUl_2Q3eVwGW3SCLUVyqPCJYwRVbtlh8Np5D6Kg8130_provenance.