Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion> ?p ?o ?g. }
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- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion type Assertion NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_head.
- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.
- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion evidence source_evidence_literature NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.
- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion SIO_000772 18024811 NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.
- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion wasDerivedFrom befree-20140225 NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.
- NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion wasGeneratedBy ECO_0000203 NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.