http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#head http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#assertion http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#provenance http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#assertion http://rdf.disgenet.org/resource/gda/DGN5cc48fec77170998f2fc951860dc0bf6 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5727 http://rdf.disgenet.org/resource/gda/DGN5cc48fec77170998f2fc951860dc0bf6 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1862314 http://rdf.disgenet.org/resource/gda/DGN5cc48fec77170998f2fc951860dc0bf6 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#provenance http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#assertion http://purl.org/dc/terms/description [The identification of t(9;16)(q22;p13) as a primary chromosomal abnormality in a subset of BCCs (we found it in 3 of 22 tumors) is especially intriguing against the background that the PTCH gene, which when mutated in the germ line presumably gives rise to the autosomal dominant basal cell nevus or Gorlin's syndrome, maps to chromosome band 9q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#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/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/9012465 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#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/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/dc/terms/created 2017-10-17T13:15:44+02:00 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP870991.RAmrMbk6ky6DZktsDSl1no_wPxl7PaRuW-If0Na_6vPJY 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