Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion> ?p ?o ?g. }
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- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion type Assertion NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_head.
- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion description "[Patients homozygous for the W1282X mutation (n = 16) and patients heterozygous for the delta F508 and W1282X mutations (n = 22) had similarly severe disease, reflected by pancreatic insufficiency, high incidence of meconium ileus (37% and 27%, respectively), early age at diagnosis, poor nutritional status, and variable pulmonary function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_provenance.
- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion evidence source_evidence_literature NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_provenance.
- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion SIO_000772 1370365 NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_provenance.
- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion wasDerivedFrom befree-20140225 NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_provenance.
- NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_assertion wasGeneratedBy ECO_0000203 NP784685.RAsggf5xcGTXglnph9Xi79RZ6Tno-Nxocu_iSj3qrNcMg130_provenance.