Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_assertion description "[Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_assertion evidence source_evidence_curated NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_assertion SIO_000772 23623389 NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_assertion wasDerivedFrom uniprot-20150221 NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_assertion wasGeneratedBy ECO_0000218 NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1284.RAktejLHNCOPefsp2QuG3_0sE0EPLXESHwYS4TqFaSteM130_provenance.