Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_assertion description "[Biallelic mutation of BEST1 causes a distinct retinopathy in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_assertion evidence source_evidence_curated NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_assertion SIO_000772 18179881 NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_assertion wasDerivedFrom uniprot-20130724 NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_assertion wasGeneratedBy ECO_0000218 NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP731.RAPYk74uSwghWx8fWhfG_wRBmvEzXncVupeJRLeueWlw4130_provenance.