Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_assertion description "[Our study identified haplotypes in the chromosomal region encompassing the KIAA0391 and PSMA6 genes as a possible genetic link between CAD and MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_assertion evidence source_evidence_literature NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_assertion SIO_000772 19624571 NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_assertion wasDerivedFrom befree-20140225 NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_assertion wasGeneratedBy ECO_0000203 NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.
- befree-20140225 importedOn "2014-02-25" NP874936.RAGupLh_NYm-_S2Jg5bTd3ugIVfV00YShZFEYp-NOO878130_provenance.