Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP406885.RAOLpE6vGqkd4Dr0KMIxoe7SYhsv2bWeZPIN2l8hMO5-w130_provenance.