Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- befree-2016 importedOn "2016-02-19" NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_assertion wasGeneratedBy ECO_0000203 NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_assertion wasDerivedFrom befree-2016 NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_assertion SIO_000772 10408773 NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_assertion evidence source_evidence_literature NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.
- NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_assertion description "[Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257919.RAtz2VYjU_7yBI8U2UfprCBhonGN9X1GqcaPQM16D-MR4130_provenance.