Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_assertion description "[Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_assertion evidence source_evidence_literature NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_assertion SIO_000772 17262171 NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_assertion wasDerivedFrom befree-20140225 NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_assertion wasGeneratedBy ECO_0000203 NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP202755.RAZc1dy0TZCPaE8oFiXOmVj05g0M1np94Hna2oT7Vq6KQ130_provenance.