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- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion type Assertion NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_head.
- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion description "[Our results therefore support the exclusion of ATP2B3 as the causal disease gene of XLMTM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_provenance.
- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion evidence source_evidence_literature NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_provenance.
- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion SIO_000772 8931700 NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_provenance.
- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion wasDerivedFrom befree-2016 NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_provenance.
- NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_assertion wasGeneratedBy ECO_0000203 NP1362962.RAs_uWfUnp9coV7yly2wJ0b8Byr97OKeXSVTH6mmdv-lw130_provenance.