Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion> ?p ?o ?g. }
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- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion type Assertion NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_head.
- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion description "[Charcot-Marie-Tooth disease type 4J (OMIM 611228) is a recessive, potentially severe form of the disease caused by mutations of the lipid phosphatase FIG4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_provenance.
- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion evidence source_evidence_literature NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_provenance.
- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion SIO_000772 21705420 NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_provenance.
- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion wasDerivedFrom befree-2016 NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_provenance.
- NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_assertion wasGeneratedBy ECO_0000203 NP904977.RAZ3PwQmARRZeSebqNlR2rkYvHzX-VMbpd3K4f6WeebQA130_provenance.