Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_assertion description "[The CD18 AvaII polymorphic site not associated with Henoch-Sch�nlein purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_assertion evidence source_evidence_literature NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_assertion SIO_000772 21269583 NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_assertion wasDerivedFrom befree-20150227 NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_assertion wasGeneratedBy ECO_0000203 NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP517722.RABxpDU0_JwlAedcZ8RP-rbLLNPM6AC6rSfKucXC4kRoU130_provenance.