Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_assertion description "[Furthermore it is related to axial skeleton and leads to wedging of vertebral bodies, with shorter dorsal margins than the ventral margins.Bartels et al. defined mutations in NPR2 gene, encoding natriuretic peptide receptor B (NPR-B), underlying Acromesomelic dysplasia, type Maroteaux.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_assertion evidence source_evidence_literature NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_assertion SIO_000772 26349192 NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_assertion wasDerivedFrom befree-2016 NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_assertion wasGeneratedBy ECO_0000203 NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293803.RA0X00Q0iG71qbkAeh5AOSeNXbdfz3fn47dBZOugOMSNQ130_provenance.