Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_assertion description "[These results extend our previous observations and indicate that defects in XPCC cause Xeroderma pigmentosum group C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_assertion evidence source_evidence_curated NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_assertion SIO_000772 8298653 NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_assertion wasDerivedFrom uniprot-2016 NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_assertion wasGeneratedBy ECO_0000218 NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8837.RA_maUK-9y6BQenurx3z-GgTGe-Ihs9EBkV3n335-AIx4130_provenance.