Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_assertion description "[Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_assertion evidence source_evidence_curated NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_assertion SIO_000772 11440989 NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_assertion wasDerivedFrom uniprot-2016 NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_assertion wasGeneratedBy ECO_0000218 NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1508.RAbH9FM3ug4Vsr1zJAUvD30mOVVdkrw1fo6PsNYlI03Cc130_provenance.