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- source_evidence_literature type ECO_0000212 NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_assertion description "[A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_assertion evidence source_evidence_literature NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_assertion SIO_000772 20932824 NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_assertion wasDerivedFrom befree-20150227 NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_assertion wasGeneratedBy ECO_0000203 NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP334031.RAT_2UxJetWdMQaOHE_sw0smkFqlyNTjgLuRxMN71mxq0130_provenance.