Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion> ?p ?o ?g. }
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- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion type Assertion NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_head.
- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_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." NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_provenance.
- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion evidence source_evidence_curated NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_provenance.
- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion SIO_000772 20170900 NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_provenance.
- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion wasDerivedFrom uniprot-2016 NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_provenance.
- NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_assertion wasGeneratedBy ECO_0000218 NP6123.RAapIxRwH3xMaqIlgi1XWc1-6tYMgGRTjn3bFynm8hAb0130_provenance.