Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_assertion description "[Multiple osteochondromas (MO) is an autosomal dominant hereditary disorder caused by heterozygous germline mutations in the exostonsin-1 (EXT1) or exostosin-2 (EXT2) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_assertion evidence source_evidence_literature NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_assertion SIO_000772 23629877 NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_assertion wasDerivedFrom befree-20140225 NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_assertion wasGeneratedBy ECO_0000203 NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212252.RAUbLh-XqkANh9D6pkwISeBEZacteIREaETENTWA0IWls130_provenance.