Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_assertion description "[We describe six different mutations of the SRD5A2 gene detected in three children with genital ambiguity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_assertion evidence source_evidence_literature NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_assertion SIO_000772 18350250 NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_assertion wasDerivedFrom befree-2016 NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_assertion wasGeneratedBy ECO_0000203 NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.
- befree-2016 importedOn "2016-02-19" NP661468.RAkFtPXQp9_sYsqcfqQrlhOyg-dfp9xDOMGtZ7Zsp6sfo130_provenance.