Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_assertion description "[This same repeat expansion was identified in the majority of our families with a combined FTD/ALS phenotype and TDP-43-based pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_assertion evidence source_evidence_literature NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_assertion SIO_000772 21944778 NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_assertion wasDerivedFrom befree-20140225 NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_assertion wasGeneratedBy ECO_0000203 NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724112.RA7E1ehSjP66VICmsfuU5tYPsyWoTF5oL7nmdQIOS4bQ4130_provenance.