Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion evidence source_evidence_literature NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion SIO_000772 16000300 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion wasDerivedFrom befree-20140225 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion wasGeneratedBy ECO_0000203 NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.