http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#head
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#assertion
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#provenance
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#assertion
http://rdf.disgenet.org/resource/gda/DGN8d3de008dbeaefc4dd0e277b37ce0855
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4647
http://rdf.disgenet.org/resource/gda/DGN8d3de008dbeaefc4dd0e277b37ce0855
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0271097
http://rdf.disgenet.org/resource/gda/DGN8d3de008dbeaefc4dd0e277b37ce0855
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#provenance
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#assertion
http://purl.org/dc/terms/description
[A custom HaloPlex panel for Illumina platforms was designed to capture all exons of the 10 known causative Usher syndrome genes (MYO7A, USH1C, CDH23, PCDH15, USH1G, CIB2, USH2A, GPR98, DFNB31 and CLRN1), the two Usher syndrome-related genes (HARS and PDZD7) and the two candidate genes VEZT and MYO15A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#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/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/25404053
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#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/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/dc/terms/created
2017-10-17T13:14:55+02:00
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP741672.RAPjEOMR2Y-FWblmNvzE_V3ZGG4xz2fwMTb_ljogHZ8CE
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