Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_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." NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_assertion evidence source_evidence_curated NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_assertion SIO_000772 21990111 NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_assertion wasDerivedFrom uniprot-20130724 NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_assertion wasGeneratedBy ECO_0000218 NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP1218.RAtQOsUOsXKfDzP0tq57CTYXUtyzMn8gygBnSkRJw19rQ130_provenance.