http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#head
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#provenance
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://rdf.disgenet.org/resource/gda/DGN50a88b958141bfa08af5b2983618236c
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/3753
http://rdf.disgenet.org/resource/gda/DGN50a88b958141bfa08af5b2983618236c
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0022387
http://rdf.disgenet.org/resource/gda/DGN50a88b958141bfa08af5b2983618236c
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#provenance
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://purl.org/dc/terms/description
[Data on the Jervell and Lange-Nielsen syndrome (J-LN), the long-QT syndrome (LQTS) variant associated with deafness and caused by homozygous or compound heterozygous mutations on the KCNQ1 or on the KCNE1 genes encoding the I(Ks) current, are still based largely on case reports.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/16461811
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/dc/terms/created
2017-10-17T13:14:05+02:00
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP613870.RANri1bNmw5mC_H9JWaxCMGSspYNiGJxshf85xv9TB7Bs
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0