http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#head
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#provenance
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://rdf.disgenet.org/resource/gda/DGNdd58a5e0d99d7817988d05e7e66706e1
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/54790
http://rdf.disgenet.org/resource/gda/DGNdd58a5e0d99d7817988d05e7e66706e1
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0023467
http://rdf.disgenet.org/resource/gda/DGNdd58a5e0d99d7817988d05e7e66706e1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#provenance
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://purl.org/dc/terms/description
[We initially identified deletions or mutations in TET2 in three patients with myelodysplastic syndromes, in three of five patients with myeloproliferative disorders, in two patients with primary AML, and in one patient with secondary AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#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/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/19474426
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/GAD
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/GAD
http://purl.org/pav/importedOn
2017-02-21
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/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/dc/terms/created
2017-10-17T13:18:36+02:00
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1325147.RAFwPxQhY1L_gg0U66B9AXG0K_UFGGMyP8HpQ65wHN-_w
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