Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_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." NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_assertion evidence source_evidence_literature NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_assertion SIO_000772 23182804 NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_assertion wasDerivedFrom befree-20140225 NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_assertion wasGeneratedBy ECO_0000203 NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.
- befree-20140225 importedOn "2014-02-25" NP763698.RAkEzmAVylDdjdpt3Z4Cvo7YGEtBn-QeGhPmIKfe_BYew130_provenance.