Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_assertion description "[VLGR1 mutations have been previously identified in both humans and mice and are associated with a reflex-seizure phenotype in both species.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_assertion evidence source_evidence_literature NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_assertion SIO_000772 14740321 NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_assertion wasDerivedFrom befree-20140225 NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_assertion wasGeneratedBy ECO_0000203 NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP556326.RAeigc-nFcYMzgC2fjB34G4-OCsWcZNJtXkt0w7X7Tt3g130_provenance.