Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_assertion description "[Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_assertion evidence source_evidence_literature NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_assertion SIO_000772 23182804 NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_assertion wasDerivedFrom befree-20150227 NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_assertion wasGeneratedBy ECO_0000203 NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP616719.RACO5nxlt8S5XeVDp1A7XO3Pt0LeF_SO5MKsBS57oTPsM130_provenance.