Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_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." NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_assertion evidence source_evidence_literature NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_assertion SIO_000772 23182804 NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_assertion wasDerivedFrom befree-20150227 NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_assertion wasGeneratedBy ECO_0000203 NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP639701.RAaD9GH7O6xBSFaVzYpPFB73fyHu4dVwwBq_gpUaDV_4I130_provenance.