Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_assertion description "[Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_assertion evidence source_evidence_literature NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_assertion SIO_000772 25175347 NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_assertion wasDerivedFrom befree-20150227 NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_assertion wasGeneratedBy ECO_0000203 NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP956002.RAjDaYgkxmGrkHCKNtodUYFg_Jc_Y6E5NTU9ve7SxuHlI130_provenance.