Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion> ?p ?o ?g. }
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- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion type Assertion NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_head.
- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion description "[Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_provenance.
- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion evidence source_evidence_curated NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_provenance.
- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion SIO_000772 15286788 NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_provenance.
- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion wasDerivedFrom uniprot-20150221 NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_provenance.
- NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_assertion wasGeneratedBy ECO_0000218 NP3860.RAE8CgmYiCtQIVVJe_9ajC7keyWYXf69Ika3mn-yVMDok130_provenance.