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- source_evidence_literature type ECO_0000212 NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_assertion description "[Based on recent studies of the photoreceptor-specific ABC transporter gene ABCR (ABCA4) in Stargardt disease (STGD1) and other retinal dystrophies, we and others have developed a model in which the severity of retinal disease correlates inversely with residual ABCR activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_assertion evidence source_evidence_literature NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_assertion SIO_000772 11379881 NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_assertion wasDerivedFrom befree-20140225 NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_assertion wasGeneratedBy ECO_0000203 NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207079.RA65jL6_0fP2T5uEKN476DTkXN2Y4wvXmXjjHtzd-E_EU130_provenance.