Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_assertion description "[Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_assertion evidence source_evidence_literature NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_assertion SIO_000772 7649547 NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_assertion wasDerivedFrom befree-2016 NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_assertion wasGeneratedBy ECO_0000203 NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316495.RAfmsmB1qNJshAiXU51v_K4Vgb66p7h0a1VGEAtou_HHs130_provenance.