Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_assertion wasGeneratedBy ECO_0000203 NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_assertion wasDerivedFrom lhgdn-20090331 NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_assertion SIO_000772 15537666 NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_assertion evidence source_evidence_literature NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.
- NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_assertion description "[Familial and sporadic forms of Pseudohypoparathyroidism type IB have distinct GNAS imprinting patterns that occur through different defects in the imprinting mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210928.RAU2l-60Qzeuv66hw5rvjWEIg4idz2AKcSbkhFpSB0WBo130_provenance.