Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_assertion description "[A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_assertion evidence source_evidence_literature NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_assertion SIO_000772 25439727 NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_assertion wasDerivedFrom befree-20150227 NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_assertion wasGeneratedBy ECO_0000203 NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP955404.RAZ7Ob30iBbRgQw64JNyPXzGeX9otr4HsIY22HZJnQAcM130_provenance.