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- source_evidence_literature type ECO_0000212 NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_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." NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_assertion evidence source_evidence_literature NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_assertion SIO_000772 22946725 NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_assertion wasDerivedFrom befree-20140225 NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_assertion wasGeneratedBy ECO_0000203 NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP609313.RAAQlGHq5tCiT_2gZD_U7RlYwb5luAOb6_U1RizsSMryw130_provenance.