Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion> ?p ?o ?g. }
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- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion type Assertion NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_head.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion evidence source_evidence_literature NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion SIO_000772 11438991 NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion wasDerivedFrom befree-20150227 NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion wasGeneratedBy ECO_0000203 NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.