Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_assertion description "[Among them, CNTN4, CADPS2, SUMF1, SLC9A9, NTRK3 have been previously implicated in autism, whereas others have been implicated in neurological disorders comorbid with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_assertion evidence source_evidence_literature NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_assertion SIO_000772 23715297 NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_assertion wasDerivedFrom befree-20140225 NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_assertion wasGeneratedBy ECO_0000203 NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP492463.RA4AvX1_NeVCgHouO3CaO4-gF2R-LtW09-K_VuCI5xFAM130_provenance.