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- source_evidence_literature type ECO_0000212 NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17 (CMT1A), chromosome 1 (CMT1B) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_assertion evidence source_evidence_literature NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_assertion SIO_000772 10219749 NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_assertion wasDerivedFrom befree-2016 NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_assertion wasGeneratedBy ECO_0000203 NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP251189.RAIt7dYxOoxTqerLiC6HyQsWu3U15UMEK4fi_4XVpjxiQ130_provenance.