Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion> ?p ?o ?g. }
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- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion type Assertion NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_head.
- 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.
- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion evidence source_evidence_literature NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_provenance.
- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion SIO_000772 11180757 NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_provenance.
- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion wasDerivedFrom befree-20140225 NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_provenance.
- NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_assertion wasGeneratedBy ECO_0000203 NP265028.RA7KSFk90j54vnP8Q30_hTfgJNUbK7zP1OB_G3ypUbS1o130_provenance.