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- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion type Assertion NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_head.
- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion wasGeneratedBy ECO_0000203 NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_provenance.
- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion wasDerivedFrom befree-20140225 NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_provenance.
- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion SIO_000772 9120678 NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_provenance.
- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion evidence source_evidence_literature NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_provenance.
- NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_assertion description "[Exon- and intron-specific polymerase chain reaction amplification of the 11 beta-HSD2 gene from genomic DNA from members of a consanguinous kindred with AME consistently revealed a single missense mutation (C1228T) in two affected sibs and twin stillbirths.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP464624.RAhDF4nlMpuIPo8zvIDmQUzEsJPb541akUgpdgGaQQIZI130_provenance.