Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion> ?p ?o ?g. }
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- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion type Assertion NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_head.
- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion description "[The V363I variation was associated with frontotemporal dementia only in the proband which was also homozygous for the A allele of the progranulin single-nucleotide polymorphism rs9897526 and for methionine at codon 129 of the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_provenance.
- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion evidence source_evidence_literature NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_provenance.
- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion SIO_000772 21343707 NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_provenance.
- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion wasDerivedFrom befree-2016 NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_provenance.
- NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_assertion wasGeneratedBy ECO_0000203 NP874350.RAm2cS6YsY2GAq0w-8SUGXMcFc73_l7-zxQOklIItv72k130_provenance.