Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion> ?p ?o ?g. }
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- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion type Assertion NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_head.
- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion wasGeneratedBy ECO_0000203 NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_provenance.
- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion wasDerivedFrom lhgdn-20090331 NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_provenance.
- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion SIO_000772 19106752 NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_provenance.
- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion evidence source_evidence_literature NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_provenance.
- NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_assertion description "[Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201459.RA8AfGhWgj1PBpp8n2PZyKnh4kAPSalehhaToglsflM0g130_provenance.