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- source_evidence_literature type ECO_0000212 NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_assertion description "[Different loci have been Identified for ectrodactyly (SHFM1 at 7q21.3q22.1, SHFM2 at Xq26, SHFM3 at 10q24q25, SHFM4 at 3q27), and two genes are known (DSS1 for SHFM1, p63 for SHFM4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_assertion evidence source_evidence_literature NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_assertion SIO_000772 12416640 NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_assertion wasDerivedFrom befree-20150227 NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_assertion wasGeneratedBy ECO_0000203 NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768074.RA_Xl2ixChTELbb1nIoQZAd1JTJyJ4MAblkRFcLxDw_OA130_provenance.