http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#head
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#assertion
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#provenance
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#assertion
http://rdf.disgenet.org/resource/gda/DGNfaaa6cb6c75059b5b6cbc3ff4f1333a8
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4137
http://rdf.disgenet.org/resource/gda/DGNfaaa6cb6c75059b5b6cbc3ff4f1333a8
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0751265
http://rdf.disgenet.org/resource/gda/DGNfaaa6cb6c75059b5b6cbc3ff4f1333a8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#provenance
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#assertion
http://purl.org/dc/terms/description
[The MAPT H1 haplotype has been associated with progressive supranuclear palsy, corticobasal degeneration, Parkinson's disease and Alzheimer's disease, while the H2 is linked to recurrent deletion events associated with the 17q21.31 microdeletion syndrome, a disease characterized by developmental delay and learning disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#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/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/22950410
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#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/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/dc/terms/created
2017-10-17T13:14:25+02:00
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP666075.RAbHq5jGKZHL8CYkCeUkRHs2EYTt9VfCbkeZM8xuu9Q7E
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