Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_assertion description "[ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_assertion evidence source_evidence_literature NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_assertion SIO_000772 20335603 NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_assertion wasDerivedFrom befree-2016 NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_assertion wasGeneratedBy ECO_0000203 NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.
- befree-2016 importedOn "2016-02-19" NP802353.RAwXSeFZghYd7qTFTvbnCnmtlzLgBTJYwfIv1mfkDSX8A130_provenance.