Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion> ?p ?o ?g. }
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- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion type Assertion NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_head.
- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.
- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion evidence source_evidence_curated NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.
- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion SIO_000772 10739753 NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.
- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion wasDerivedFrom ctd_human-20130708 NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.
- NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion wasGeneratedBy ECO_0000218 NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.