Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_assertion description "[Several of the top candidate genes include EEF1A1, ROBO1, PLXNA4, SLIT3, NRP1, and NOTCH2, as well as genes associated with the Usher syndrome, PCDH15 and USH2A, and are plausible candidates contributing to the developmental defects in Gbx2(-/-) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_assertion evidence source_evidence_literature NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_assertion SIO_000772 23144817 NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_assertion wasDerivedFrom befree-20140225 NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_assertion wasGeneratedBy ECO_0000203 NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP336882.RAD_Y9tIS7qfV8nFSlB1oQc52u43SJeG4Jh42hQLMB5eQ130_provenance.