http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#head
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#assertion
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#provenance
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#assertion
http://rdf.disgenet.org/resource/gda/DGNde0c9e2aca358d351841f3374f5b6e4c
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/2332
http://rdf.disgenet.org/resource/gda/DGNde0c9e2aca358d351841f3374f5b6e4c
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0032897
http://rdf.disgenet.org/resource/gda/DGNde0c9e2aca358d351841f3374f5b6e4c
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#provenance
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#assertion
http://purl.org/dc/terms/description
[Mutational analysis of MECP2 was performed in mentally retarded female patients who were negative for FMR1 CGG repeat expansion, in male and female patients with clinical features suggestive of either Angelman or Prader-Willi syndrome without methylation defects on chromosome 15q11-q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#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/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/14560307
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#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/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/dc/terms/created
2017-10-17T13:12:48+02:00
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412425.RAKJpWXKew0XzJYXeNgsZjcPih_PULMogaxJ-dz8VEnmo
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