Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_assertion description "[These findings suggest that polymorphisms in MMP2, MMP3, MMP-13, and ELN genes may independently contribute to the pathogenesis of AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_assertion evidence source_evidence_literature NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_assertion SIO_000772 22094117 NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_assertion wasDerivedFrom befree-2016 NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_assertion wasGeneratedBy ECO_0000203 NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.
- befree-2016 importedOn "2016-02-19" NP939526.RAGETzIIXp9MNNTa-wIeRFf4KPhEK8X7v2A_OGGJRfLGs130_provenance.