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- source_evidence_literature type ECO_0000212 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), while mutations in multiple genes cause autosomal dominant DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion evidence source_evidence_literature NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion SIO_000772 14567970 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion wasDerivedFrom befree-20140225 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_assertion wasGeneratedBy ECO_0000203 NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP793415.RAC4lx2pT2EBG-JYyN8f60URCs52_QWobJOdyp-Wg8A2k130_provenance.