Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion> ?p ?o ?g. }
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- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion type Assertion NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_head.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion wasGeneratedBy ECO_0000203 NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion wasDerivedFrom gad-20150221 NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion SIO_000772 20513142 NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion evidence source_evidence_literature NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.
- NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_assertion description "[the phenotypic overlap of patients with MEF2C mutations and atypical Rett syndrome is due to the involvement of a common pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177473.RAuJc4F4iDIe7LfipHSQ5SgpKn-qMNDnGQdtM_M6dLN_c130_provenance.