Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_assertion description "[It is noteworthy that contrary to a previous study, we did not find an association between the MMP9 (nt-1562) polymorphism and AAA, suggesting genetic heterogeneity of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_assertion evidence source_evidence_literature NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_assertion SIO_000772 15944607 NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_assertion wasDerivedFrom gad-20130706 NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_assertion wasGeneratedBy ECO_0000203 NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP54386.RA1rOLyEm36p3G1IeiX71F5PC_d2CbusDrdoCqvX6IqhA130_provenance.