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- source_evidence_literature type ECO_0000212 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion description "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion evidence source_evidence_literature NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion SIO_000772 9690138 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion wasDerivedFrom befree-20140225 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion wasGeneratedBy ECO_0000203 NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.