http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#head
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#assertion
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#provenance
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#assertion
http://rdf.disgenet.org/resource/gda/DGNd8aad4d56afcab274407b42987238ef5
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1540
http://rdf.disgenet.org/resource/gda/DGNd8aad4d56afcab274407b42987238ef5
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C1857941
http://rdf.disgenet.org/resource/gda/DGNd8aad4d56afcab274407b42987238ef5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#provenance
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#assertion
http://purl.org/dc/terms/description
[Haplotype analysis was performed for the Spanish patients with MFT1, Dutch patients with FC and an Austrian patient with BSS, all of whom carry the same heterozygous nonsense p.R758X CYLD mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#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/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/26861065
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#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/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/dc/terms/created
2017-10-17T13:11:51+02:00
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP260178.RAQsYIqfiyFBEKUSJlrfomHpxSoCTpH2Tz53EK1QIXm9w
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