@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:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_head { this: np:hasAssertion dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_assertion; np:hasProvenance dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_provenance; np:hasPublicationInfo dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_publicationInfo; a np:Nanopublication . dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_assertion a np:Assertion . dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_provenance a np:Provenance . dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_publicationInfo a np:PublicationInfo . } dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_assertion { miriam-gene:7276 a ncit:C16612 . lld:C0032580 a ncit:C7057 . dgn-gda:DGN5bcf70898c820f37c3cee1818fe2ea6f sio:SIO_000628 miriam-gene:7276, lld:C0032580; a sio:SIO_001122 . } dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_provenance { dgn-np:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_assertion dcterms:description "[The data suggest that the onset of symptoms of FAP V30M may be modulated by an interval downstream of TTR on the accompanying noncarrier chromosome (defined by microsatellites D18S457 and D18S456), but not by the immediately 5'- and 3'-flanking sequences of TTR.]. 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:14673473; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP424401.RA4hhGYbau7zeXFqrQ7Z8t3WO4o_q-0xLI9m2YF93NEag130_publicationInfo { this: dcterms:created "2016-05-13T12:44:57+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }