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- source_evidence_literature type ECO_0000212 NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_assertion description "[Thirty-two Brazilian families with MODY phenotype were screened for GCK and HNF1A mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_assertion evidence source_evidence_literature NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_assertion SIO_000772 25174781 NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_assertion wasDerivedFrom befree-2016 NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_assertion wasGeneratedBy ECO_0000203 NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215509.RAl4DufUrX5_JyknSmnYSeuhsLF_IU3CrVk-aNfbsgSg8130_provenance.