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- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion type Assertion NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_head.
- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion wasGeneratedBy ECO_0000203 NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_provenance.
- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion wasDerivedFrom lhgdn-20090331 NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_provenance.
- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion SIO_000772 11748844 NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_provenance.
- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion evidence source_evidence_literature NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_provenance.
- NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_assertion description "[The most frequent mutation in this study was the previously reported M467T and it was also detected in the normal population with an allelic frequency of 0.5%, which implies that other genes may be involved in cystinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216751.RAcLSrc6Tj9aH-6P4NYUjxGJV2sA1iAp5pvwOjw2ggVoE130_provenance.