http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#head http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#assertion http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#provenance http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#assertion http://rdf.disgenet.org/resource/gda/DGN302510747c463a0f9b6dd17e367a5286 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2260 http://rdf.disgenet.org/resource/gda/DGN302510747c463a0f9b6dd17e367a5286 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1563720 http://rdf.disgenet.org/resource/gda/DGN302510747c463a0f9b6dd17e367a5286 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#provenance http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#assertion http://purl.org/dc/terms/description [The recent finding that FGFR1 mutations are involved in an autosomal dominant form of Kallmann syndrome (KAL2), combined with the analysis of mutant mouse embryos that no longer express Fgfr1 in the telencephalon, suggests that the disease results from a deficiency in FGF signaling at the earliest stage of olfactory bulb morphogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#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/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/15365636 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#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/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/dc/terms/created 2017-10-17T13:12:42+02:00 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP395812.RAVom8KGx3Sd1kVVsz0Ey5JWCOX5vuVoKnMZFXoczwmf4 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