Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_assertion description "[MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_assertion evidence source_evidence_literature NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_assertion SIO_000772 18781619 NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_assertion wasDerivedFrom befree-2016 NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_assertion wasGeneratedBy ECO_0000203 NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.
- befree-2016 importedOn "2016-02-19" NP692244.RAOWAbAlvobJJwTLARUVCnMXYyLrVGPCJWZL0dK1-J9c0130_provenance.