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- source_evidence_literature type ECO_0000212 NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_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." NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion evidence source_evidence_literature NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion SIO_000772 24754450 NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion wasDerivedFrom befree-2016 NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion wasGeneratedBy ECO_0000203 NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_provenance.