Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_assertion description "[The MMP9 C(-1562)T and TNFA C(-863)A SNP were associated with severe weakness and poor outcome, indicating that these SNP may be one of the factors predisposing to a severe form of GBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_assertion evidence source_evidence_literature NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_assertion SIO_000772 17761309 NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_assertion wasDerivedFrom befree-20150227 NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_assertion wasGeneratedBy ECO_0000203 NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP747613.RABXXVeMmUIPIWrAI-Y4kI94E9ji25yWQMNVGgPQtXTO0130_provenance.