Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion> ?p ?o ?g. }
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- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion type Assertion NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_head.
- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_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." NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_provenance.
- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion evidence source_evidence_literature NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_provenance.
- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion SIO_000772 16647572 NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_provenance.
- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion wasDerivedFrom gad-20150221 NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_provenance.
- NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_assertion wasGeneratedBy ECO_0000203 NP100347.RAueldc-E6EPb4HVo7K7CBLxdvs1o9ihx9sBkbPhSafOc130_provenance.