Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_assertion description "[Charcot-Marie-Tooth disease Type 2A2 (CMT2A2), caused by mitofusin 2 (MFN2) genes, has been clinically classified into two types: severe early-onset and mild benign.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_assertion evidence source_evidence_literature NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_assertion SIO_000772 22762946 NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_assertion wasDerivedFrom befree-2016 NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_assertion wasGeneratedBy ECO_0000203 NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.
- befree-2016 importedOn "2016-02-19" NP995190.RA0d0lblTgY-Ud0XWK1NeRO2qYowcgTFpcISwx952koj8130_provenance.