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- source_evidence_literature type ECO_0000212 NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_assertion description "[Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with unusual multisystemic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_assertion evidence source_evidence_literature NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_assertion SIO_000772 12601109 NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_assertion wasDerivedFrom befree-20150227 NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_assertion wasGeneratedBy ECO_0000203 NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782585.RA_9-uaiwR_iRl6nD_-oPYVMicjgCtEqN_1OXG_ds_Ln0130_provenance.