Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion> ?p ?o ?g. }
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- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion type Assertion NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_head.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion description "[As this is a third independent case of protein C Tochigi with thromboembolism, the mutation of Arg169 (CGG) to Trp169 (TGG) in the protein C gene may be a hot spot and a common type of genetic lesion in congenital protein C deficiency with thromboembolic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion evidence source_evidence_literature NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion SIO_000772 1596024 NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion wasDerivedFrom befree-2016 NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_assertion wasGeneratedBy ECO_0000203 NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.