Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.