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- source_evidence_literature type ECO_0000212 NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_assertion description "[Our goal is to identify a rapid, efficient and cost effective mutation detection method for the molecular diagnosis of MODY and other human genetic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_assertion evidence source_evidence_literature NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_assertion SIO_000772 11440371 NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_assertion wasDerivedFrom befree-20150227 NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_assertion wasGeneratedBy ECO_0000203 NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP461318.RA8NrnGUPUahx9z6G1ocXixe0YKGv4XJD-gZvz4-zfQW8130_provenance.