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- source_evidence_literature type ECO_0000212 NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- befree-2016 importedOn "2016-02-19" NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_assertion wasGeneratedBy ECO_0000203 NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_assertion wasDerivedFrom befree-2016 NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_assertion SIO_000772 15741255 NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_assertion evidence source_evidence_literature NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.
- NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_assertion description "[In a patient with HLRCC caused by a germline-inactivating FH mutation, we diagnosed atypical (subclinical) CS due to bilateral, ACTH-independent adrenocortical hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483347.RA3QWRP6_fjx-8eAuMT0Az18EbN_-1iiFMbHnXSy5he2A130_provenance.