Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP803338.RAQ0HBbsKOmpU-cQ98Ic0QltD8kJM1bbysfx2MIxBXu50130_provenance.