Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_assertion description "[Charcot-Marie-Tooth neuropathy (CMT) type 1 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." NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_assertion evidence source_evidence_literature NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_assertion SIO_000772 7804455 NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_assertion wasDerivedFrom befree-20140225 NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_assertion wasGeneratedBy ECO_0000203 NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP674760.RAziwPLRRUa27HcfyKdzCFu4hc9NrWaowKSbUi8WD1h7w130_provenance.