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- source_evidence_literature type ECO_0000212 NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_assertion description "[Our results provide new evidence that genetic polymorphisms of PLA2R1 may be the underlying cause of IMN, and the polymorphisms revealed by this study warrant further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_assertion evidence source_evidence_literature NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_assertion SIO_000772 20937089 NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_assertion wasDerivedFrom befree-2016 NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_assertion wasGeneratedBy ECO_0000203 NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.
- befree-2016 importedOn "2016-02-19" NP844809.RAVXUnhxBgq6j_hOUoHA6up2ilTLcjMFqy8t4h6LarfsE130_provenance.