Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_assertion description "[Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_assertion evidence source_evidence_curated NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_assertion SIO_000772 21990111 NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_assertion wasDerivedFrom uniprot-20150221 NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_assertion wasGeneratedBy ECO_0000218 NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1226.RAUlwfhYONs0d56SKy2m-5DbphWl2LyqbKTqMccDVNG-Y130_provenance.