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- source_evidence_literature type ECO_0000212 NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion evidence source_evidence_literature NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion SIO_000772 24754450 NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion wasDerivedFrom befree-20150227 NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_assertion wasGeneratedBy ECO_0000203 NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257104.RAfMtaUkWBXq8yGUZpTe0yS-dceU82TGFGXY9_W__U9ko130_provenance.