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- source_evidence_literature type ECO_0000212 NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion evidence source_evidence_literature NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion SIO_000772 9302264 NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion wasDerivedFrom befree-2016 NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_assertion wasGeneratedBy ECO_0000203 NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1380695.RAnwGA57A-qML2-_2zrKptueMrwk5O1zyZKNVC_hNzMGY130_provenance.