Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion> ?p ?o ?g. }
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- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion type Assertion NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_head.
- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion description "[Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_provenance.
- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion evidence source_evidence_curated NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_provenance.
- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion SIO_000772 20170900 NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_provenance.
- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion wasDerivedFrom uniprot-20130724 NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_provenance.
- NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_assertion wasGeneratedBy ECO_0000218 NP601.RAlFlcDqe_CNk65ROFAjrThYdp_dO8mZ1jnQrYMaLwOcc130_provenance.