Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion evidence source_evidence_literature NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion SIO_000772 18438698 NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion wasDerivedFrom befree-20140225 NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion wasGeneratedBy ECO_0000203 NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.