Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_assertion description "[In combination with PGC-1 alpha genotypes, 3.8% additional residual variance in HD AO can be explained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_assertion evidence source_evidence_literature NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_assertion SIO_000772 20108082 NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_assertion wasDerivedFrom befree-2016 NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_assertion wasGeneratedBy ECO_0000203 NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.
- befree-2016 importedOn "2016-02-19" NP790003.RAV9mzAcuXy3qMQkNBQ5T_An_C7hcvFrSzxWCrZr3loRY130_provenance.