Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion> ?p ?o ?g. }
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- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion type Assertion NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_head.
- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion wasGeneratedBy ECO_0000203 NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion wasDerivedFrom befree-20140225 NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion SIO_000772 10438713 NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion evidence source_evidence_literature NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_assertion description "[X-linked dyskeratosis congenita (DC) is a bone marrow failure syndrome caused by mutations in the DKC1 gene located at Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.