Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion wasGeneratedBy ECO_0000218 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion wasDerivedFrom uniprot-2016 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion SIO_000772 22961002 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion evidence source_evidence_curated NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.