Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_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." NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_assertion evidence source_evidence_curated NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_assertion SIO_000772 21990111 NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_assertion wasDerivedFrom uniprot-2016 NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_assertion wasGeneratedBy ECO_0000218 NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6806.RA0O14nXR4XRAldW2xjB6FYiTB7jRnP18QLqmiuWm3Kq4130_provenance.