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- source_evidence_literature type ECO_0000212 NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_assertion description "[Single-nucleotide polymorphism genotyping for C282Y (rs1800562) and H63D (rs1799945) HFE mutations was performed in 786 adult subjects in the NASH Clinical Research Network (CRN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_assertion evidence source_evidence_literature NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_assertion SIO_000772 22611049 NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_assertion wasDerivedFrom befree-20150227 NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_assertion wasGeneratedBy ECO_0000203 NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP447358.RAIeIaUefEp_0IpNoMN8Au7NsN0CoSqBDJsASAAS5LbSg130_provenance.