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- source_evidence_literature type ECO_0000212 NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_assertion description "[This raises the question whether the CNS disorders of XPA, XPB, and XPD patients are similar, or whether a careful clinical evaluation might reveal different mechanisms of development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_assertion evidence source_evidence_literature NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_assertion SIO_000772 10699759 NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_assertion wasDerivedFrom befree-2016 NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_assertion wasGeneratedBy ECO_0000203 NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.
- befree-2016 importedOn "2016-02-19" NP276870.RAsVKXuxA4O6fQBt1aEmWyLJ160Q4HJBL6LafpMWJrQ5g130_provenance.