Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_assertion description "[Cathepsin C gene: First compound heterozygous patient with Papillon-Lefvre syndrome and a novel symptomless mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_assertion evidence source_evidence_curated NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_assertion SIO_000772 11180601 NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_assertion wasDerivedFrom uniprot-20130724 NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_assertion wasGeneratedBy ECO_0000218 NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP1610.RAqLGEsy49sSMVZs95VG9Q3G5yUu6jaKfzN7MjhAPn7y0130_provenance.