@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:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_head { this: np:hasAssertion dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_assertion; np:hasProvenance dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_provenance; np:hasPublicationInfo dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_publicationInfo; a np:Nanopublication . dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_assertion a np:Assertion . dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_provenance a np:Provenance . dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_assertion { miriam-gene:9172 a ncit:C16612 . lld:C0025007 a ncit:C7057 . dgn-gda:DGNd67510d43aa05ac722815427e266baad sio:SIO_000628 miriam-gene:9172, lld:C0025007; a sio:SIO_001122 . } dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_provenance { dgn-np:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_assertion dcterms:description "[Some of these mutations like the L165P found in the M protein sequence of the Laine strain, the amino acid position 94, where a mutation M94V was found in the F protein sequence of the Hoedts strain are known to play an important role in the glycoprotein interaction and to impair the ability of measles virus strain to produce cell-free infectious viral particles.This is the first study on molecular characterization of the entire coding region of measles virus isolated from SSPE cases in France.]. 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:21739453; 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:NP816770.RAM7O3Pzusk-2mWMq7a3v8lJBs5U65TKcFXMlO0sOyZlQ130_publicationInfo { this: dcterms:created "2015-08-25T14:45:55+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" . }