Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_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." NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_assertion evidence source_evidence_literature NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_assertion SIO_000772 23144817 NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_assertion wasDerivedFrom befree-2016 NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_assertion wasGeneratedBy ECO_0000203 NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027790.RAPeTlY9vpsBKRw9TQyOTXp95Mss0Zabfb0Z4MH_i1_yM130_provenance.