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- source_evidence_literature type ECO_0000212 NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP499908.RAcPX23jnXjL0ibw4RU_Rguo2dZ0eCEeIRZFKAi89Y7BI130_provenance.