Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_assertion description "[For example, mutations in CLN5, CLN6, MFSD8, or CLN8 can underlie the clinically similar late infantile variant NCL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_assertion evidence source_evidence_curated NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_assertion SIO_000772 21990111 NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_assertion wasDerivedFrom uniprot-2016 NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_assertion wasGeneratedBy ECO_0000218 NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6811.RA4Lgu91bGoae_Z7Mt0XDhJvZc2RLUy7SlFx1ETCe9w2c130_provenance.