Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion type Assertion NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_head.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion description "[Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome in which the known susceptibility genes (DKC1, TERC, and TERT) belong to the telomere maintenance pathway; patients with DC have very short telomeres.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_provenance.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion evidence source_evidence_literature NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_provenance.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion SIO_000772 17468339 NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_provenance.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion wasDerivedFrom befree-20140225 NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_provenance.
- NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_assertion wasGeneratedBy ECO_0000203 NP261626.RAsMiSkchyfJv7uLtkzAkZzG6KweDYsoXqt6jx7L0YWv0130_provenance.