Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a genetically heterogeneous group of chronic demyelinating polyneuropathies with loci mapping to chromosome 17p (CMT1A), chromosome 1q (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." NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_assertion evidence source_evidence_literature NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_assertion SIO_000772 7952853 NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_assertion wasDerivedFrom befree-2016 NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_assertion wasGeneratedBy ECO_0000203 NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1328100.RAPF3J1-5S2CZAG6QkrvqktG2_Ck1SE0bJKPVPP6b0Vgo130_provenance.