@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_head { this: np:hasAssertion dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_assertion; np:hasProvenance dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_provenance; np:hasPublicationInfo dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_publicationInfo; a np:Nanopublication . dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_assertion a np:Assertion . dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_provenance a np:Provenance . dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_publicationInfo a np:PublicationInfo . } dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_assertion { miriam-gene:83886 a ncit:C16612 . lld:C0032463 a ncit:C7057 . dgn-gda:DGN5876c91dde22ca42cd667e30b8c837e9 sio:SIO_000628 miriam-gene:83886, lld:C0032463; a sio:SIO_001122 . } dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_provenance { dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_assertion dcterms:description "[Therefore, we examined 108 Japanese patients with MPN, including 19 with PV, 61 with ET, 10 with PMF, and 17 with unclassifiable MPN, as well as 104 control individuals for the JAK2 rs10974944(C/G) single nucleotide polymorphism, in which the G allele indicates the 46/1 haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:23430670; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP953900.RA-IT_FYSva7Cv1JPmwnA_zCDIvjiaSPywSPBJkbviGkc130_publicationInfo { this: dcterms:created "2015-08-25T14:47:22+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }