Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_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." NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_assertion evidence source_evidence_literature NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_assertion SIO_000772 9399908 NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_assertion wasDerivedFrom befree-20140225 NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_assertion wasGeneratedBy ECO_0000203 NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP486699.RANmv1JDl_PjC9zzA-EJ6pSwmIORvbmfJObOyuo0G3wwc130_provenance.