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- source_evidence_literature type ECO_0000212 NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_assertion description "[Most people with HH are C282Y homozygotes, a small proportion are compound heterozygotes or H63D homozygotes, and some have no identifiable HFE mutation or are HFE heterozygotes, suggesting that additional mutations associated with HH are yet to be found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_assertion evidence source_evidence_literature NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_assertion SIO_000772 9727731 NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_assertion wasDerivedFrom befree-2016 NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_assertion wasGeneratedBy ECO_0000203 NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1403383.RARg2DSrd0dn9MR178sIQAk2CKnFcfocnQFEICAXpWvmM130_provenance.