Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_assertion description "[Initial linkage studies with color blindness (CB), glucose-6-phosphate dehydrogenase (G6PD) deficiency, and the blood coagulation factor IX (F9) have suggested that a gene for BP illness is located in the Xq27-q28 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_assertion evidence source_evidence_literature NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_assertion SIO_000772 7726217 NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_assertion wasDerivedFrom befree-2016 NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_assertion wasGeneratedBy ECO_0000203 NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319740.RAda6Uw0o8bJZBnzRqGEkJ7JXXxXSV-YtGs5YS0yCsm_w130_provenance.