Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion> ?p ?o ?g. }
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- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion type Assertion NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_head.
- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion description "[Most COL2A1 mutations occur in the triple helical region of alpha 1(II) chains: the SED spectrum is mostly attributed to missense mutations that substitute bulky amino acids for glycine residues, STD-I to haploinsufficiency of truncation mutations, and KND to exon skipping due to splice-site mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_provenance.
- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion evidence source_evidence_literature NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_provenance.
- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion SIO_000772 15895462 NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_provenance.
- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion wasDerivedFrom befree-2016 NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_provenance.
- NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_assertion wasGeneratedBy ECO_0000203 NP494931.RAos1YHFX9FwjaJMMSyaIa9hQprQ56jPn8NN1UpNPqlyE130_provenance.