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- source_evidence_literature type ECO_0000212 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion description "[Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion evidence source_evidence_literature NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion SIO_000772 17959774 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion wasDerivedFrom befree-2016 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_assertion wasGeneratedBy ECO_0000203 NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.
- befree-2016 importedOn "2016-02-19" NP637063.RAbaZNzyn3Uu8rNqn4OJyPPmALvc_UvOiotaAyEIbFryY130_provenance.