http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#head http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#assertion http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#provenance http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#assertion http://rdf.disgenet.org/resource/gda/DGN13a4b02a70260dc32f4866ce70989742 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6469 http://rdf.disgenet.org/resource/gda/DGN13a4b02a70260dc32f4866ce70989742 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0004779 http://rdf.disgenet.org/resource/gda/DGN13a4b02a70260dc32f4866ce70989742 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#provenance http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#assertion http://purl.org/dc/terms/description [Loss-of-function mutations in Patched (Ptch1) are implicated in constitutive activation of the Sonic hedgehog pathway in human basal cell carcinomas (BCCs), and inherited Ptch1 mutations underlie basal cell nevus syndrome in which a typical feature is multiple BCC occurring with greater incidence in portals of radiotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#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/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/14871823 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#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/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/dc/terms/created 2017-10-17T13:16:11+02:00 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP942653.RA0kIAHe5mmnChbUbWCFFrgA_Yq5OVtGTydwr_OXxgujY 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