@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:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_head { this: np:hasAssertion dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion; np:hasProvenance dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance; np:hasPublicationInfo dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo; a np:Nanopublication . dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion a np:Assertion . dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance a np:Provenance . dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion { miriam-gene:6647 a ncit:C16612 . lld:C1862939 a ncit:C7057 . dgn-gda:DGN0ff6c07da520a64bfa4ef50ea2102b44 sio:SIO_000628 miriam-gene:6647, lld:C1862939; a sio:SIO_001121 . } dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance { dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion dcterms:description "[The discovery of mutations in the human SOD1 gene encoding Cu,Zn superoxide dismutase (Cu,Zn SOD) in patients with familial amyotrophic lateral sclerosis (ALS) has made possible the development of etiological models of the 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:9419057; 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:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo { this: dcterms:created "2016-05-13T12:52:14+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" . }