Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_assertion description "[Functional analysis of HNPCC-related missense mutations in MSH2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_assertion evidence source_evidence_curated NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_assertion SIO_000772 18822302 NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_assertion wasDerivedFrom uniprot-20130724 NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_assertion wasGeneratedBy ECO_0000218 NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP4156.RAIw3RRk6hO7rM2CEn0hNOLJWAz8ms_VgXbPZXBmI0GM0130_provenance.