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- source_evidence_literature type ECO_0000212 NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_assertion description "[In addition, we report four K12 mutations in Meesmann corneal epithelial dystrophy (MCD), an autosomal dominant disorder characterized by intraepithelial microcysts and corneal epithelial fragility in which mutations in keratin 3 (K3) and K12 have recently been implicated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_assertion evidence source_evidence_literature NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_assertion SIO_000772 9399908 NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_assertion wasDerivedFrom befree-2016 NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_assertion wasGeneratedBy ECO_0000203 NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1385440.RA2i_kFy2pJXcOaWly34c9-7x2MeE06CaVzM_4oF7IE3Y130_provenance.