Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_assertion description "[These data strongly implicate MYLK genetic variants to confer increased risk of sepsis and sepsis-associated ALI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_assertion evidence source_evidence_literature NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_assertion SIO_000772 16399953 NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_assertion wasDerivedFrom befree-20150227 NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_assertion wasGeneratedBy ECO_0000203 NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583931.RAfYlt8W5OG9NXXIeGEaeTZNJwZbN1ggGWClN2d4x4e4o130_provenance.