Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion wasGeneratedBy ECO_0000203 NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion wasDerivedFrom befree-20140225 NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion SIO_000772 14644728 NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion evidence source_evidence_literature NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion description "[The absence of systemic features was characteristic of the vitreoretinopathies linked to chromosome 5q13 (Wagner disease and erosive vitreoretinopathy) and mutations in exon 2 of the COL2A1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_provenance.