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- source_evidence_literature type ECO_0000212 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion description "[The chromatin-associated protein ATRX was originally identified because mutations in the ATRX gene cause a severe form of syndromal X-linked mental retardation associated with alpha-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion evidence source_evidence_literature NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion SIO_000772 17609377 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion wasDerivedFrom befree-2016 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_assertion wasGeneratedBy ECO_0000203 NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.
- befree-2016 importedOn "2016-02-19" NP618352.RAXHZmqV7eBEgPklTl14-ixuRYt-h-Tw1_kPhT5K5fQWI130_provenance.