http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#head
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#assertion
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#provenance
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#assertion
http://rdf.disgenet.org/resource/gda/DGN8d4872012ab214640690e927bd2d16cf
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/5979
http://rdf.disgenet.org/resource/gda/DGN8d4872012ab214640690e927bd2d16cf
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0238462
http://rdf.disgenet.org/resource/gda/DGN8d4872012ab214640690e927bd2d16cf
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#provenance
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#assertion
http://purl.org/dc/terms/description
[Results showed the benefit of systematic RET mutation screening in HD patients in order to identify the risk of MTC in preclinical stage of the disease in patients with HD and their family members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#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/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/17021738
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#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/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/dc/terms/created
2017-10-17T13:15:57+02:00
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP905675.RA1L2y9iqge2x8t-8rNiAxTgKbJi67PI_vDRs4ylCMDBk
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