http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#head http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#assertion http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#provenance http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#assertion http://rdf.disgenet.org/resource/gda/DGN94e1b5949fc93336810736620dabf403 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/64324 http://rdf.disgenet.org/resource/gda/DGN94e1b5949fc93336810736620dabf403 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0004352 http://rdf.disgenet.org/resource/gda/DGN94e1b5949fc93336810736620dabf403 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#provenance http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#assertion http://purl.org/dc/terms/description [Our findings suggest that Sotos syndrome is a rare cause of autism spectrum disorders and that screening for NSD1 mutations and deletions in patients with autism and macrocephaly is not warranted in the absence of other features of Sotos syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#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/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18001468 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#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/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/dc/terms/created 2017-10-17T13:18:50+02:00 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1361856.RAh936mEhNDN_HY45KVPqfZATX6Y-FzjO6ejH_DwrwKbk 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