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- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_assertion type Assertion NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_head.
- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_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." NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_provenance.
- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_assertion evidence source_evidence_literature NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_provenance.
- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_assertion SIO_000772 19136952 NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_provenance.
- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_assertion wasDerivedFrom befree-20150227 NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_provenance.
- NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_assertion wasGeneratedBy ECO_0000203 NP844756.RAVOE6-pDQtL_I-IirDF6577Paq-MW4ns9Loh2Up1mSTc130_provenance.