Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP218970.RA8v6q0zsHRQ8F8qDfB9uFWIkp673OJwOc4ooQNpPuDBw130_provenance.