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- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion type Assertion NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_head.
- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion wasGeneratedBy ECO_0000203 NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_provenance.
- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion wasDerivedFrom befree-2016 NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_provenance.
- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion SIO_000772 17083511 NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_provenance.
- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion evidence source_evidence_literature NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_provenance.
- NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_assertion description "[Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577667.RA6bq3ohbf3LSrNJLtIznSiMUvwd5SXb4AI7SQKZhs9Wo130_provenance.