Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_assertion description "[Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_assertion evidence source_evidence_literature NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_assertion SIO_000772 18085567 NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_assertion wasDerivedFrom befree-2016 NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_assertion wasGeneratedBy ECO_0000203 NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.
- befree-2016 importedOn "2016-02-19" NP645627.RAT_-QUuHVGYkpigEmyJzw06snABCkbMMxXu9wgyrKeHM130_provenance.