Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_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), the X chromosome (CMTX) and to another unknown autosome (CMT1C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_assertion evidence source_evidence_literature NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_assertion SIO_000772 7849745 NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_assertion wasDerivedFrom befree-2016 NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_assertion wasGeneratedBy ECO_0000203 NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323783.RAiu_st7nBo8FRinocgHo2LaualtXlUVPfMbJRR1hNIaU130_provenance.