http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#head
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#assertion
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#provenance
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#assertion
http://rdf.disgenet.org/resource/gda/DGNf39019b0fdef3e320a7bcfc35502d80e
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1188
http://rdf.disgenet.org/resource/gda/DGNf39019b0fdef3e320a7bcfc35502d80e
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0004775
http://rdf.disgenet.org/resource/gda/DGNf39019b0fdef3e320a7bcfc35502d80e
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#provenance
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#assertion
http://purl.org/dc/terms/description
[Neonatal Bartter's syndrome is caused by mutations of NKCC2 or ROMK, classic Bartter's syndrome by mutations of ClC-Kb, Bartter's syndrome associated with sensorineural deafness is due to mutations of BSND, Gitelman's syndrome to mutations of NCCT and Bartter's syndrome associated with autosomal dominant hypocalcemia is linked to mutations of CASR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#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/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/15056980
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#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/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/dc/terms/created
2017-10-17T13:11:35+02:00
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP218640.RAZw0qY6YosLch6sTsD7DtZjw2LeUpeWPfNEqzLqCn0fU
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