Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_assertion description "[Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_assertion evidence source_evidence_literature NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_assertion SIO_000772 25155093 NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_assertion wasDerivedFrom befree-2016 NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_assertion wasGeneratedBy ECO_0000203 NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1213669.RA4Kaa_48chv36BD3kzvJ_yVxGtXDD8l97aEOpO1XjLpw130_provenance.