Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_assertion description "[Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_assertion evidence source_evidence_literature NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_assertion SIO_000772 11012604 NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_assertion wasDerivedFrom befree-2016 NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_assertion wasGeneratedBy ECO_0000203 NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.
- befree-2016 importedOn "2016-02-19" NP296385.RA8F9ZgZBda803J51j06hFRul2wvCt6VQoBXj2ck3OQHM130_provenance.