Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion> ?p ?o ?g. }
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- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion type Assertion NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_head.
- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_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." NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_provenance.
- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion evidence source_evidence_literature NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_provenance.
- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion SIO_000772 9399908 NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_provenance.
- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion wasDerivedFrom befree-2016 NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_provenance.
- NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_assertion wasGeneratedBy ECO_0000203 NP1385438.RAYR34A-8dd0Jv_D6Bmtk6Iv3Q5R4pFKkunoqBS7H39to130_provenance.