Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_assertion description "[Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_assertion evidence source_evidence_curated NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_assertion SIO_000772 8673138 NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_assertion wasDerivedFrom uniprot-2016 NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_assertion wasGeneratedBy ECO_0000218 NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9063.RAXXsQ2MIS7cbm_PwbqxgKkF6sGc08QVqA93pc8boPoCU130_provenance.