Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion> ?p ?o ?g. }
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- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion type Assertion NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_head.
- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion description "[Restudy of the original DFN-1 family showed that the deafness is part of a progressive X linked recessive syndrome, which includes visual disability leading to cortical blindness, dystonia, fractures, and mental deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_provenance.
- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion evidence source_evidence_literature NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_provenance.
- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion SIO_000772 7643352 NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_provenance.
- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion wasDerivedFrom befree-20140225 NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_provenance.
- NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_assertion wasGeneratedBy ECO_0000203 NP239238.RAVOCQEsaXewblMNGQdfmL3vKTeDzr285oRFS-Kb1EINA130_provenance.