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- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion type Assertion NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_head.
- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion wasGeneratedBy ECO_0000203 NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_provenance.
- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion wasDerivedFrom befree-2016 NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_provenance.
- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion SIO_000772 15580558 NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_provenance.
- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion evidence source_evidence_literature NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_provenance.
- NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_assertion description "[We conclude that KCNJ11 mutations are a common cause of PNDM either in isolation or associated with developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471408.RAvR3Jd85_kSg3H2TINJOzXvyU8NgFMspLpSJMBU5JC1s130_provenance.