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- source_evidence_literature type ECO_0000212 NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_assertion description "[This suggests that, consistent with a classic tumour suppressor model, carriers of damaging mutations in BAP1 are predisposed to UM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_assertion evidence source_evidence_literature NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_assertion SIO_000772 24187051 NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_assertion wasDerivedFrom befree-20150227 NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_assertion wasGeneratedBy ECO_0000203 NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759349.RAHsEhnx7b2JUWeXZr9KWG3rVwyhdf61HmX21L4-QMWKw130_provenance.