@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:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_head { this: np:hasAssertion dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_assertion; np:hasProvenance dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_provenance; np:hasPublicationInfo dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_publicationInfo; a np:Nanopublication . dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_assertion a np:Assertion . dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_provenance a np:Provenance . dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_publicationInfo a np:PublicationInfo . } dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_assertion { miriam-gene:5265 a ncit:C16612 . lld:C0221757 a ncit:C7057 . dgn-gda:DGN352750e15faaa761ca6d8962666d3424 sio:SIO_000628 miriam-gene:5265, lld:C0221757; a sio:SIO_001121 . } dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_provenance { dgn-np:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_assertion dcterms:description "[The A(1)ATVar database is the only integrated database on the Internet offering summarized information on AAT allelic variants and could be useful not only for clinical diagnosis and research on AAT deficiency and the SERPINA1 gene, but could also serve as an example for an all-in-one solution for locus-specific database (LSDB) development and curation.]. 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:19021233; 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:NP704824.RAlvB7AJdRdWB9xmPybv6fVPkw7_mjr8UZ8jOfqDahpFk130_publicationInfo { this: dcterms:created "2016-05-13T12:47:04+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" . }