Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_assertion wasGeneratedBy ECO_0000203 NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_assertion wasDerivedFrom befree-20140225 NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_assertion SIO_000772 13679292 NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_assertion evidence source_evidence_literature NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_assertion description "[Pelizeaus-Merzbacher disease (PMD) is a clinically and molecularly heterogeneous disorder linked to deletion, mutations, or duplication of the proteolipid protein (PLP1) gene locus at Xq22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP303159.RACmfY9T5pDm8KO3iwPzrRU9CjiMQ2M2qleD-K39yHpJI130_provenance.