Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_assertion description "[Other variants (GTA 118 GTC, GCGCA-->GCACA in the 3'-noncoding region, and the number of ATT repeats in intron 2) also did not associate with CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_assertion evidence source_evidence_literature NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_assertion SIO_000772 9589253 NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_assertion wasDerivedFrom befree-2016 NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_assertion wasGeneratedBy ECO_0000203 NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395258.RAoDDCU75plUU8EyG3zkRsxGi8-GQLSQXFHp2hVYl3VT8130_provenance.