Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion> ?p ?o ?g. }
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- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion type Assertion NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_head.
- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion description "[The absence of pathogenic mutations in VSX1, SOD1, COL4A3, and COL4A4 genes in our large number of unrelated keratoconus patients indicates that other genetic factors are involved in the development of this disorder; nevertheless, a significant correlation of a few polymorphisms indicates that there could be a link between specific polymorphisms and KC disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_provenance.
- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion evidence source_evidence_literature NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_provenance.
- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion SIO_000772 20664914 NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_provenance.
- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion wasDerivedFrom gad-20150221 NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_provenance.
- NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_assertion wasGeneratedBy ECO_0000203 NP114060.RAy4VOScIq5SqE0hHmCrL_WFPyTXq96BuMx0Ug0VXOT8Q130_provenance.