Matches in Nanopublications for { ?s ?p "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_provenance.
- assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP307494.RAlGcXBgW3f9xqryJ_JoddiKDm2drhWQ0_mlHUZgWOqcE130_assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307494.RAlGcXBgW3f9xqryJ_JoddiKDm2drhWQ0_mlHUZgWOqcE130_provenance.
- NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919339.RA00ftC7dpiW8Eh3qQBqps-WbzYFno9qUfkocRAKoEeNA130_provenance.
- NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_assertion description "[Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is an autosomal dominant eye movement disorder linked to the pericentromere of chromosome 12 (12p11.2 - q12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307492.RA243cz0VafCNrFluRl1Q5VZrifR0rWakJ13N5kdB1F4E130_provenance.