http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#head
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#assertion
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#provenance
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#assertion
http://rdf.disgenet.org/resource/gda/DGN85b3fd55910af7520e4d1d92d6730785
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/8988
http://rdf.disgenet.org/resource/gda/DGN85b3fd55910af7520e4d1d92d6730785
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C3711384
http://rdf.disgenet.org/resource/gda/DGN85b3fd55910af7520e4d1d92d6730785
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#provenance
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#assertion
http://purl.org/dc/terms/description
[Recently, mutations in both the small heat shock protein 27 (HSP27 or HSPB1) and 22 (HSP22 or HSPB8) genes have been reported to cause autosomal dominant CMT with minimal sensory involvement (CMT 2F/CMT2L) and autosomal dominant distal hereditary motor neuropathy type II (dHMN II).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#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/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18832141
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#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/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/dc/terms/created
2017-10-17T13:17:38+02:00
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1169449.RAVISRyB_bAf5Kl82iafnq-88EpD1QH8ol8boP51XGikI
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