Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_assertion description "[To describe a novel mutation in TRK-fused gene (TFG) as a new cause of dominant axonal Charcot-Marie-Tooth disease (CMT) identified by exome sequencing and further characterized by in vitro functional studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_assertion evidence source_evidence_literature NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_assertion SIO_000772 25098539 NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_assertion wasDerivedFrom befree-2016 NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_assertion wasGeneratedBy ECO_0000203 NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1208184.RAPMSmnWgoVP2LovJ42xjgu_RS7OU_I4-dei6lOU92Y-Y130_provenance.