Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion> ?p ?o ?g. }
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- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion type Assertion NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_head.
- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion description "[To identify the disease locus associated with autosomal dominant Fuchs corneal dystrophy (FCD) in a large family and to compare the progression of severity in families mapped to the FCD1 and FCD2 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_provenance.
- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion evidence source_evidence_literature NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_provenance.
- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion SIO_000772 19608540 NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_provenance.
- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion wasDerivedFrom befree-20140225 NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_provenance.
- NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_assertion wasGeneratedBy ECO_0000203 NP722849.RArT5Ll2BT0Re4VJ7Cx_zQJnBQoTAQrMk8OcFFtfYFXYA130_provenance.