Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- befree-20150227 importedOn "2015-02-27" NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_assertion wasGeneratedBy ECO_0000203 NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_assertion wasDerivedFrom befree-20150227 NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_assertion SIO_000772 17466001 NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_assertion evidence source_evidence_literature NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.
- NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_assertion description "[Patients lacked mutations in other genes known to cause ACTH resistance, including AAAS for patients diagnosed with triple A syndrome and MC2R and MRAP for patients diagnosed with familial glucocorticoid deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922995.RAqAIU4l9LtvM_if3EnDZlr062sl1k6vVWYyYvf_4nsok130_provenance.