Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_assertion description "[We conclude that mutations in PFN1 are not a common cause for ALS/FTLD in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_assertion evidence source_evidence_literature NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_assertion SIO_000772 23182804 NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_assertion wasDerivedFrom befree-20140225 NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_assertion wasGeneratedBy ECO_0000203 NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP727475.RADTXIqJDXYP4FCV3AW-ZlukC8FeEoTKWe_4bX84qjN4c130_provenance.