Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion> ?p ?o ?g. }
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- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion type Assertion NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_head.
- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion description "[Such rare CDKN1B variants may contribute to the development of pituitary adenomas, but their low incidence and lack of clear segregation with affected patients make CDKN1B sequencing unlikely to be of use in routine genetic investigation of FIPA kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.
- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion evidence source_evidence_literature NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.
- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion SIO_000772 22291433 NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.
- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion wasDerivedFrom befree-20150227 NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.
- NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion wasGeneratedBy ECO_0000203 NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance.