Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion wasGeneratedBy ECO_0000203 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion wasDerivedFrom befree-2016 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion SIO_000772 24848304 NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion evidence source_evidence_literature NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.
- NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_assertion description "[Netherton syndrome (NS; OMIM 256500) is a genetic skin disease resulting from defects in the serine protease inhibitor Kazal-type 5 (SPINK5) gene, which encodes the protease inhibitor lympho-epithelial Kazal type inhibitor (LEKTI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184348.RAseX7p7xh1_ycMMOIfNv3UeCsjTB8JYFuHmlIUWa0UmU130_provenance.