Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_assertion description "[Mutations in eight genes (PPT1/CLN1, TPP1/CLN2, CLN3, CLN5, CLN6, MFSD8/CLN7, CLN8) have been identified and several more are predicted to exist, including two provisionally named CLN4 and CLN9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_assertion evidence source_evidence_curated NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_assertion SIO_000772 21990111 NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_assertion wasDerivedFrom uniprot-2016 NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_assertion wasGeneratedBy ECO_0000218 NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6812.RAqyECzBRQ4P0r5cnTh8opIHG0GCqJbzczGt8t55SF_eM130_provenance.