Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion> ?p ?o ?g. }
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- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion type Assertion NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_head.
- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion wasGeneratedBy ECO_0000203 NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.
- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion wasDerivedFrom befree-20140225 NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.
- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion SIO_000772 8734807 NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.
- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion evidence source_evidence_literature NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.
- NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_assertion description "[Glycogen storage disease type Ia (GSD Ia, von Gierke disease) is an autosomal recessive inborn error of metabolism caused by the deficiency of D-glucose-6-phosphatase (G6Pase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524457.RAU1Y4q7Q0Q1UcsGaWpijH6RsCoDU8x7I5GTKosGMwzFc130_provenance.