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- source_evidence_literature type ECO_0000212 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion evidence source_evidence_literature NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion SIO_000772 22946725 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion wasDerivedFrom befree-2016 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_assertion wasGeneratedBy ECO_0000203 NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1010131.RAtHgylO_L0foPWZl8AlcPxNRqMmEsiwUdi457wYgA7QI130_provenance.