Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_assertion description "[Importantly, in contrast to current thinking, our results suggest that imprinted genes may not underlie the SRS phenotype, and we propose an alternative hypothesis to explain the occurrence of maternal UPD 7 seen in some cases of SRS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_assertion evidence source_evidence_literature NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_assertion SIO_000772 10987657 NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_assertion wasDerivedFrom befree-20140225 NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_assertion wasGeneratedBy ECO_0000203 NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP374060.RA0ILI3tqbllb2_BHtYJ5upPZIEwLSaD_TLLO6Zdx-Zo8130_provenance.