Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion> ?p ?o ?g. }
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- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion type Assertion NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_head.
- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion description "[Autosomal recessive polycystic kidney disease (ARPKD) [MIM 263200] belongs to a group of congenital hepatorenal fibrocystic syndromes and is caused by mutations in the PKHD1 gene encoding the multidomain protein fibrocystin/polyductin (FPC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_provenance.
- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion evidence source_evidence_literature NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_provenance.
- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion SIO_000772 19176689 NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_provenance.
- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion wasDerivedFrom befree-20140225 NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_provenance.
- NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_assertion wasGeneratedBy ECO_0000203 NP273807.RAUKWFmW0FzqyczKfhMepwcDwCDSFbZc83mcvhRj0yPa8130_provenance.