Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_assertion description "[Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_assertion evidence source_evidence_literature NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_assertion SIO_000772 23623389 NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_assertion wasDerivedFrom befree-20150227 NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_assertion wasGeneratedBy ECO_0000203 NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382490.RAKVT8_ouzvME3xqmDB-VqO0ovq6HbhSJnuaHciT0WyKg130_provenance.