@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:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_head { this: np:hasAssertion dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_assertion; np:hasProvenance dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_provenance; np:hasPublicationInfo dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_publicationInfo; a np:Nanopublication . dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_assertion a np:Assertion . dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_provenance a np:Provenance . dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_assertion { miriam-gene:6647 a ncit:C16612 . lld:C0085084 a ncit:C7057 . dgn-gda:DGN0ce650e787ef51a6f5bdd5902b522f5c sio:SIO_000628 miriam-gene:6647, lld:C0085084; a sio:SIO_001121 . } dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_provenance { dgn-np:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_assertion dcterms:description "[Several SOD1 mutations have been shown by ourselves and others to cause motor neuron disease when expressed at high levels in transgenic mice, whereas transgenic mice expressing comparable amounts of wild-type human SOD do not show clinical disease.]. 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:8734301; 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:NP1354626.RAvQpq7ev0e_UaSfqkZDcZL1YqSXWjJl8xfjQZZrGMWp8130_publicationInfo { this: dcterms:created "2016-05-13T12:52:00+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" . }