Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- befree-2016 importedOn "2016-02-19" NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_assertion wasGeneratedBy ECO_0000203 NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_assertion wasDerivedFrom befree-2016 NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_assertion SIO_000772 17057786 NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_assertion evidence source_evidence_literature NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.
- NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_assertion description "[hOgg1 326C allele frequency was 21.35% (38 of 178) in the AMD group compared with 19.12% (65 of 340) in the random controls and 19.59% (38 of 194) in the age-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575642.RAp3tfQtsHQQs9Gmmhixh0OEbKP0Y0Mq-4B4hXJ72wT_s130_provenance.