Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion> ?p ?o ?g. }
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- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion type Assertion NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_head.
- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion description "[Mutations in the Stargardt disease gene (ABCR) were previously reported in patients with atrophic forms of AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_provenance.
- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion evidence source_evidence_literature NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_provenance.
- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion SIO_000772 10634626 NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_provenance.
- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion wasDerivedFrom befree-20140225 NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_provenance.
- NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_assertion wasGeneratedBy ECO_0000203 NP600698.RAE3cR1EYgv8KSUJ_BSbpUsvLDq5H6MqKhtV5RXON7_p4130_provenance.