@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:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_head { this: np:hasAssertion dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_assertion; np:hasProvenance dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_provenance; np:hasPublicationInfo dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_publicationInfo; a np:Nanopublication . dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_assertion a np:Assertion . dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_provenance a np:Provenance . dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_publicationInfo a np:PublicationInfo . } dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_assertion { miriam-gene:4041 a ncit:C16612 . lld:C0029458 a ncit:C7057 . dgn-gda:DGNcdbca753d4e198b53a5c2e157cc60366 sio:SIO_000628 miriam-gene:4041, lld:C0029458; a sio:SIO_001122 . } dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_provenance { dgn-np:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_assertion dcterms:description "[In this study, we found common polymorphisms of LRP5 associated with osteoporotic fractures, and polymorphisms of the LRP6 gene associated with BMD, thus suggesting them as likely candidates to contribute to the explaination of the hereditary influence on]. 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:20926594; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP186988.RACJ_53mqNwBBmM_TPZ0HsIDDbuibZaNJadMMItZkqn58130_publicationInfo { this: dcterms:created "2016-05-13T12:43:12+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" . }