Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_assertion description "[We also tested a primer set to detect the FUS-CREB3L1 fusion transcript, which is a rare variant of the gene fusion in LGFMS, although no PCR products were identified in any case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_assertion evidence source_evidence_literature NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_assertion SIO_000772 16931951 NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_assertion wasDerivedFrom befree-20150227 NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_assertion wasGeneratedBy ECO_0000203 NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP960562.RAIoqXTKy31v_6NcTw641RggS_dlgbMXNECRCxwJnZmVg130_provenance.