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- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion type Assertion NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_head.
- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion wasGeneratedBy ECO_0000203 NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_provenance.
- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion wasDerivedFrom lhgdn-20090331 NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_provenance.
- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion SIO_000772 16251236 NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_provenance.
- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion evidence source_evidence_literature NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_provenance.
- NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_assertion description "[ACTN4 mutations accounts for about 3.5% of familial focal glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213809.RABPRC7X8-PQ_d-DN6-6TvBXNs1OYX2wz4E5NC3Jh7CEI130_provenance.