Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion> ?p ?o ?g. }
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- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion type Assertion NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_head.
- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion description "[Recently, mutations in RAF1 have been also identified in patients with NS and two patients with LEOPARD (multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_provenance.
- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion evidence source_evidence_literature NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_provenance.
- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion SIO_000772 20052757 NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_provenance.
- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion wasDerivedFrom befree-20140225 NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_provenance.
- NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_assertion wasGeneratedBy ECO_0000203 NP338251.RAZboezapbN8IybjmBTgrCwNMTPcv04E2QdiAaVCT8uPo130_provenance.