Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_assertion description "[Mutations in the haemoglobin beta-globin (HbB) and glucose-6-phosphate dehydrogenase (G6PD) genes cause widespread human genetic disorders such as sickle cell diseases and G6PD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_assertion evidence source_evidence_literature NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_assertion SIO_000772 16356170 NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_assertion wasDerivedFrom befree-20140225 NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_assertion wasGeneratedBy ECO_0000203 NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP658961.RASudUXR8dcpdvAI9G9jvmRQxplfmD6ZEvKPKdcB9lgY4130_provenance.