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- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion type Assertion NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_head.
- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion description "[We carried out genome-wide linkage analysis and identified five disease-segregating mutations affecting the CAP-Gly domain of dynactin (encoded by DCTN1) in eight families with Perry syndrome; these mutations diminish microtubule binding and lead to intracytoplasmic inclusions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_provenance.
- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion evidence source_evidence_literature NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_provenance.
- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion SIO_000772 19136952 NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_provenance.
- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion wasDerivedFrom befree-20150227 NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_provenance.
- NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_assertion wasGeneratedBy ECO_0000203 NP873705.RAV0tQIZhGl3v4v59zyLbBmKMI6SdXFAb8i3-pS2w4QsI130_provenance.