Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion> ?p ?o ?g. }
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- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion type Assertion NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_head.
- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion description "[To screen persons with dominantly inherited HSAN I and others with idiopathic sensory neuropathies for known mutations of SPTLC1 and RAB7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion evidence source_evidence_literature NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion SIO_000772 15965219 NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion wasDerivedFrom befree-20140225 NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_assertion wasGeneratedBy ECO_0000203 NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.