Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_assertion description "[The findings encourage studying the functional effect of the identified variants on CGB expression and HCG hormone activity to elucidate further the role of CGB variation in RM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_assertion evidence source_evidence_literature NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_assertion SIO_000772 18782867 NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_assertion wasDerivedFrom befree-20140225 NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_assertion wasGeneratedBy ECO_0000203 NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP593976.RAt3NM4Lq5B8gAiM9a0ejV2pdoyWdLZ8Iiv4kHxdNEcfY130_provenance.