http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#head
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#assertion
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#provenance
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#assertion
http://rdf.disgenet.org/resource/gda/DGN3fe490af24222c603416247316629c9e
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/2332
http://rdf.disgenet.org/resource/gda/DGN3fe490af24222c603416247316629c9e
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0278061
http://rdf.disgenet.org/resource/gda/DGN3fe490af24222c603416247316629c9e
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#provenance
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#assertion
http://purl.org/dc/terms/description
[A loss-of-function mutation in the FMR1 gene leads to subtle changes in neural development and subsequent mental impairment characteristic of FX. hNPCs were isolated from fetal cortex carrying the FMR1 mutation to determine whether aberrations occur in their proliferation and differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#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/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18225979
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#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/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/dc/terms/created
2017-10-17T13:12:48+02:00
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412819.RASwM_u-mcsj816vxHI2491ZYMdek1tKeJcVetKLJRZJQ
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