Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP250882.RAne-1NpirlrQr9NGXm9XEhKTeFEEpKS7ZJ6rfIc3_Pfg130_provenance.