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- source_evidence_literature type ECO_0000212 NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_assertion description "[A high prevalence of ANO5 deficiency was found among patients with unclassified LGMD2 (46 %) and MMD (100 %).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_assertion evidence source_evidence_literature NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_assertion SIO_000772 23670307 NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_assertion wasDerivedFrom befree-20150227 NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_assertion wasGeneratedBy ECO_0000203 NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP980096.RAEQkhiJXeCXHKlt9Xf12n4u3vZqDgiHobeSIABorlNjg130_provenance.