Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion> ?p ?o ?g. }
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- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion type Assertion NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_head.
- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_provenance.
- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion evidence source_evidence_literature NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_provenance.
- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion SIO_000772 16647572 NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_provenance.
- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion wasDerivedFrom gad-20150221 NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_provenance.
- NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_assertion wasGeneratedBy ECO_0000203 NP86063.RA-iLb1Lo1LZFIUlD8EdekvDycPjhwpNOqZX61VY_VGQk130_provenance.