Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion> ?p ?o ?g. }
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- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion type Assertion NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_head.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion description "[OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion evidence source_evidence_curated NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion SIO_000772 25293953 NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion wasDerivedFrom uniprot-2016 NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.
- NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_assertion wasGeneratedBy ECO_0000218 NP8033.RAW4OoQZFrcAgedAWasN4_4mhstNYncYBeGr940O5ThrE130_provenance.