Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_assertion description "[No TARDBP mutations in a French Canadian population of patients with Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_assertion evidence source_evidence_literature NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_assertion SIO_000772 19204172 NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_assertion wasDerivedFrom gad-20130706 NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_assertion wasGeneratedBy ECO_0000203 NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP81058.RA-vR2eTxjJYK8nljjEY1QRQGHV_GNlLYnny45fnG3sbw130_provenance.