Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion> ?p ?o ?g. }
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- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion type Assertion NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_head.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion description "[A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion evidence source_evidence_literature NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion SIO_000772 7152370 NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion wasDerivedFrom befree-2016 NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.
- NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_assertion wasGeneratedBy ECO_0000203 NP1307718.RAvWHf1jQxatK6TL9Y9iodiziGLo8-JTIytYq7-x1LwWQ130_provenance.