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- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion type Assertion NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_head.
- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion wasGeneratedBy ECO_0000203 NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_provenance.
- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion wasDerivedFrom befree-2016 NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_provenance.
- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion SIO_000772 22899009 NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_provenance.
- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion evidence source_evidence_literature NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_provenance.
- NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_assertion description "[Interestingly, mutations in C16orf57 were also observed among patients diagnosed with Rothmund-Thomson syndrome (RTS) and dyskeratosis congenita (DC), which are caused by mutations in genes involved in DNA repair and telomere maintenance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005805.RA7mEZ_5dXPXmWo5ds2Mz0r1JUyyQDQgW-lc7VGQjCOEQ130_provenance.