Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion> ?p ?o ?g. }
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- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion type Assertion NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_head.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion wasGeneratedBy ECO_0000203 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion wasDerivedFrom befree-2016 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion SIO_000772 10657149 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion evidence source_evidence_literature NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion description "[New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.