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- source_evidence_literature type ECO_0000212 NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_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." NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_assertion evidence source_evidence_literature NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_assertion SIO_000772 20937089 NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_assertion wasDerivedFrom gad-20150221 NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_assertion wasGeneratedBy ECO_0000203 NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP128265.RA6hV3I8_WbL5wSz9mylPCGSmwnJCjQNotsA53QrxZhLw130_provenance.