Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion type Assertion NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_head.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion description "[Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects in humans with dominant and recessive forms of hypotrichosis-lymphedema-telangiectasia (HLT) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion evidence source_evidence_literature NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion SIO_000772 19429912 NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion wasDerivedFrom befree-20150227 NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.
- NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_assertion wasGeneratedBy ECO_0000203 NP910618.RAixuftrLCttYPmmxrjnU8kEkyAtzTZw-zY4CNPU2X-AA130_provenance.