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- source_evidence_literature type ECO_0000212 NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_assertion description "[These observations highlight the wide spectrum of CMT1A and the overlap between CMT1A and HNPP (both linked to the PMP22 gene), and finally illustrate the complexity of the genotype-phenotype correlations in Charcot-Marie-Tooth diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_assertion evidence source_evidence_literature NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_assertion SIO_000772 24792522 NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_assertion wasDerivedFrom befree-2016 NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_assertion wasGeneratedBy ECO_0000203 NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1179036.RAx5shnSzfzQyTygwdYkfpBk6V8Ar6-sdR47qDpxSiwLI130_provenance.