@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_head
{
this:
np:hasAssertion
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_assertion
;
np:hasProvenance
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_assertion
a
np:Assertion
.
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_provenance
a
np:Provenance
.
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_assertion
{
miriam-gene:3145
a
ncit:C16612
.
lld:C0162565
a
ncit:C7057
.
dgn-gda:DGN09c0dd2f7ad113858b7a7361b93bd4e7
sio:SIO_000628
miriam-gene:3145
,
lld:C0162565
;
a
sio:SIO_001121
.
}
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_provenance
{
dgn-np:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_assertion
dcterms:description
"[The PBGD mutation analysis was found to have full specificity and sensitivity and can be used as the sole diagnostic method in the family complex studied, representing the major AIP mutation in Sweden.]. 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:7891051
;
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:NP1325182.RAmbrkVPoKtVtLdlR68dr37oOK_2SHY2jx-yjEt2UeEW8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:47+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}