Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion> ?p ?o ?g. }
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- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion type Assertion NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_head.
- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion description "[Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_provenance.
- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion evidence source_evidence_literature NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_provenance.
- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion SIO_000772 25504735 NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_provenance.
- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion wasDerivedFrom befree-2016 NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_provenance.
- NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_assertion wasGeneratedBy ECO_0000203 NP1248081.RAxVQboSZrtctAEPYaVjtzv32zAqC6UCnszD4xzYq7MqU130_provenance.