Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_assertion description "[In recent papers published by our group, we described the associations between the single nucleotide polymorphisms (SNPs) AADAT +401C?>?T, APEX1 Asn148Glu, OGG1 Ser326Cys and PARP1 Val762Ala and BM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_assertion evidence source_evidence_literature NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_assertion SIO_000772 26316174 NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_assertion wasDerivedFrom befree-2016 NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_assertion wasGeneratedBy ECO_0000203 NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293355.RAXVC_ICkuQKNBBX_quTVQqmdZ8GvsYSSoG65zwNfLQes130_provenance.