http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#head http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#assertion http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#provenance http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#assertion http://rdf.disgenet.org/resource/gda/DGN880314ad143fac16ad85f1331a6268be http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/128674 http://rdf.disgenet.org/resource/gda/DGN880314ad143fac16ad85f1331a6268be http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0162809 http://rdf.disgenet.org/resource/gda/DGN880314ad143fac16ad85f1331a6268be http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#provenance http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#assertion http://purl.org/dc/terms/description [Some cases of mutations of FGFR1, and more rarely of its ligand FGF8, or of PROKR2 or its ligand PROK2 have been shown in women suffering from Kallmann syndrome or its hyposmic or normosmic variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#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/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/20363464 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#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/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/dc/terms/created 2017-10-17T13:19:05+02:00 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1402804.RAQNlzMYi68j3L4FJu_TrlysxT4N37uVdBw9eKwQKzUvI 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