Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_assertion evidence source_evidence_literature NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_assertion SIO_000772 17903297 NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_assertion wasDerivedFrom gad-20150221 NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_assertion wasGeneratedBy ECO_0000203 NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.
- gad-20150221 importedOn "2015-02-21" NP112747.RASbvTizCLsferuuq6BmD4PucMUJRzcVtU_jZRzczKn5k130_provenance.