@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:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_head { this: np:hasAssertion dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_assertion; np:hasProvenance dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_provenance; np:hasPublicationInfo dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_publicationInfo; a np:Nanopublication . dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_assertion a np:Assertion . dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_provenance a np:Provenance . dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_publicationInfo a np:PublicationInfo . } dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_assertion { miriam-gene:4923 a ncit:C16612 . lld:C0019159 a ncit:C7057 . dgn-gda:DGN43e855b458a32eeb99f72473a122797e sio:SIO_000628 miriam-gene:4923, lld:C0019159; a sio:SIO_001121 . } dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_provenance { dgn-np:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_assertion dcterms:description "[To determine whether differences in HAV are related to the wide range of clinical severity, we used PCR-single strand conformation polymorphism (SSCP) to analyze the amplified product of the 5'-nontranslated region (5'NTR), where relatively homologous sequences are reported and the internal ribosomal entry site is considered to exist, from these various levels of hepatitis A. Twenty-seven patients admitted to Chiba University Hospital (between 1988 and 1997) were examined for HAV RNA in their sera by RT-PCR with primers located at 5'NTR of HAV RNA.]. 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:11258569; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP322556.RAne6Ha7NmYf8qu2MFGLY-4kSsxBJ2NHh-9U8rGfD5Vi8130_publicationInfo { this: dcterms:created "2014-10-02T12:35:08+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }