Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_assertion description "[Missense mutations in this gene result in HSD10 deficiency, whereas a silent mutation results in mental retardation, X-linked, syndromic 10 (MRXS10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_assertion evidence source_evidence_literature NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_assertion SIO_000772 22132097 NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_assertion wasDerivedFrom befree-2016 NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_assertion wasGeneratedBy ECO_0000203 NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP943145.RAeEQwWFN8aRkYueYLjhuxWENn2U29limpYrUoX5pJqOU130_provenance.