Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_assertion description "[A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_assertion evidence source_evidence_curated NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_assertion SIO_000772 7757079 NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_assertion wasDerivedFrom uniprot-2016 NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_assertion wasGeneratedBy ECO_0000218 NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8489.RA-d7PZ207ccejQzFFFYEGKhO7ciXDoi8miAV1Hdz5NV4130_provenance.