Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion wasGeneratedBy ECO_0000203 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion wasDerivedFrom befree-20140225 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion SIO_000772 23840040 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion evidence source_evidence_literature NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- befree-20140225 importedOn "2014-02-25" NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.