Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion evidence source_evidence_literature NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion SIO_000772 10657149 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion wasDerivedFrom befree-2016 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_assertion wasGeneratedBy ECO_0000203 NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.
- befree-2016 importedOn "2016-02-19" NP273982.RAt82bKHBhnVja90Hg98sqEEPcd9hI-Beg2WKunRr931A130_provenance.