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- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion type Assertion NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_head.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion wasGeneratedBy ECO_0000203 NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion wasDerivedFrom lhgdn-20090331 NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion SIO_000772 15304595 NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion evidence source_evidence_literature NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.
- NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190205.RAOfjuyM0hSLPAzvrfoJVsjGQLFvDpsQHKciuxIV8x0PQ130_provenance.