Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion> ?p ?o ?g. }
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- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion type Assertion NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_head.
- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion description "[To report clinical, neuroradiologic, neurophysiologic, and genetic findings on 16 patients from 11 unrelated families with a remarkable uniform phenotype characterized by infantile ascending hereditary spastic paralysis (IAHSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion evidence source_evidence_literature NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion SIO_000772 12601111 NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion wasDerivedFrom befree-20140225 NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_assertion wasGeneratedBy ECO_0000203 NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.