Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_assertion wasGeneratedBy ECO_0000203 NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_assertion wasDerivedFrom befree-20150227 NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_assertion SIO_000772 23339108 NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_assertion evidence source_evidence_literature NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.
- NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_assertion description "[To date, mutations in IFT80, DYNC2H1, TTC21B and WDR19 have been reported in ATD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945661.RACdBWiAmd6xUBrZi2wRYWs3xuhCJmxELH53KOwwQlhYQ130_provenance.