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- source_evidence_literature type ECO_0000212 NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_assertion description "[The authors found that using both exome sequencing and allele frequency data from large sequencing efforts may aid genetic diagnosis of MH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_assertion evidence source_evidence_literature NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_assertion SIO_000772 24013571 NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_assertion wasDerivedFrom befree-20150227 NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_assertion wasGeneratedBy ECO_0000203 NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP929693.RAb27inWGqZlO7_BgK-2zWpHZMXNOR5PznO3dV02INP4E130_provenance.