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- source_evidence_literature type ECO_0000212 NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_assertion description "[Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_assertion evidence source_evidence_literature NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_assertion SIO_000772 9399908 NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_assertion wasDerivedFrom befree-2016 NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_assertion wasGeneratedBy ECO_0000203 NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1385437.RAVm1PU65fcmB9g32xrV79Kmi0Hvzm-pkls6pYf5RXPbQ130_provenance.