Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion> ?p ?o ?g. }
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- NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_assertion type Assertion NP313699.RAYy3Hmi-UztRbtkCZT3_TH2OboRalYDmKv-eUjhSaGU4130_head.
- 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.