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- source_evidence_literature type ECO_0000212 NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_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." NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_assertion evidence source_evidence_literature NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_assertion SIO_000772 16931951 NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_assertion wasDerivedFrom befree-2016 NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_assertion wasGeneratedBy ECO_0000203 NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.
- befree-2016 importedOn "2016-02-19" NP565953.RAPmTfRCSq50OAgaPJz199HCwxeg8g4XD5SYf6QuOtdVE130_provenance.