http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#head
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#assertion
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#provenance
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#assertion
http://rdf.disgenet.org/resource/gda/DGN84721501116ce2b1ba0ca7b1f506fe6b
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/57492
http://rdf.disgenet.org/resource/gda/DGN84721501116ce2b1ba0ca7b1f506fe6b
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0037822
http://rdf.disgenet.org/resource/gda/DGN84721501116ce2b1ba0ca7b1f506fe6b
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#provenance
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#assertion
http://purl.org/dc/terms/description
[Taken together with published data, these results indicate that haploinsufficiency of the ARID1B gene, which encodes an epigenetic modifier of chromatin structure, is an important cause of CSS and is potentially a common cause of intellectual disability and speech impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#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/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/22426309
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#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/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/dc/terms/created
2017-10-17T13:18:45+02:00
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1348936.RAUqfHs5ocorP6_YM9gSl17KfO93mQHws7XROI3yFyk5c
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