Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion> ?p ?o ?g. }
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- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion type Assertion NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_head.
- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion wasGeneratedBy ECO_0000203 NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_provenance.
- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion wasDerivedFrom befree-20140225 NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_provenance.
- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion SIO_000772 24115768 NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_provenance.
- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion evidence source_evidence_literature NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_provenance.
- NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_assertion description "[Mutations in CTC1 lead to the telomere syndromes Coats Plus and dyskeratosis congenita (DC), but the molecular mechanisms involved remain unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508385.RAxfkPMjEopFUbj81CQVIB_hP0V4WmRCnavYvpL4irxIk130_provenance.