Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion> ?p ?o ?g. }
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- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion type Assertion NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_head.
- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion description "[Autosomal recessive Stargardt disease (STGD1) is a macular dystrophy caused by mutations in the ABCA4 (ABCR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion evidence source_evidence_literature NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion SIO_000772 18463687 NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion wasDerivedFrom befree-20150227 NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_assertion wasGeneratedBy ECO_0000203 NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.