Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_assertion type Assertion NP1175635.RA5cfBxgJY9B7QZQsy9N2G0_4zdM4PzGcZk8gzXzD7Gm0130_head.
- 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.