Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion description "[This indel mutation in FHL1 broadens the spectrum of FHL1-related disorders and implicates it in the pathogenesis of NS spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion evidence source_evidence_literature NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion SIO_000772 23456229 NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion wasDerivedFrom befree-20140225 NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion wasGeneratedBy ECO_0000203 NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_provenance.