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- source_evidence_literature type ECO_0000212 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion evidence source_evidence_literature NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion SIO_000772 17959774 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion wasDerivedFrom lhgdn-20090331 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_assertion wasGeneratedBy ECO_0000203 NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215497.RAt8SqvgFjxfl6emluv5iXdH6OodzA_SMKxhf9tiMUDKI130_provenance.