Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion> ?p ?o ?g. }
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- NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_assertion type Assertion NP517908.RAZvUzYTtjXkeRvwEQMmv2r61J1HB9jRIqpc_PfMxqu3E130_head.
- 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.