Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion description "[Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion evidence source_evidence_literature NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion SIO_000772 25502226 NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion wasDerivedFrom befree-2016 NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_assertion wasGeneratedBy ECO_0000203 NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247723.RAkCOlH4YVF0PY9E6PWueFIFk8nO4UKE1TjSmD2SBKk2o130_provenance.