Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_assertion evidence source_evidence_literature NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_assertion SIO_000772 19507262 NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_assertion wasDerivedFrom befree-2016 NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_assertion wasGeneratedBy ECO_0000203 NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.
- befree-2016 importedOn "2016-02-19" NP744034.RAxNds1-JYltm-MinTXLRI5BWHJ5vmKA1p1lG5yPU2Oj0130_provenance.