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- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion type Assertion NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_head.
- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion description "[The more common X-linked recessive form of EDMD is caused by mutations in either EMD (encoding emerin) or FHL1 (encoding four and a half LIM domains 1), while mutations in LMNA (encoding lamin A/C), SYNE1 (encoding nesprin-1) and SYNE2 (encoding nesprin-2) lead to autosomal dominant forms of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_provenance.
- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion evidence source_evidence_literature NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_provenance.
- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion SIO_000772 23456229 NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_provenance.
- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion wasDerivedFrom befree-20150227 NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_provenance.
- NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_assertion wasGeneratedBy ECO_0000203 NP373891.RA8RIRG2L4oYuf4zgHp-fkcvH7Q9HArsiAv2fkJ2Olrqo130_provenance.