Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_assertion wasGeneratedBy ECO_0000203 NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_assertion wasDerivedFrom befree-2016 NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_assertion SIO_000772 23840040 NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_assertion evidence source_evidence_literature NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.
- NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_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." NP1092584.RAfOJH0OXGteYvL7HslUd_PExakMos_Lpz1sqtfIk317Q130_provenance.