@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA
> .
@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/v3.0.0/void/
> .
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_head
{
this:
np:hasAssertion
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_assertion
;
np:hasProvenance
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_provenance
;
np:hasPublicationInfo
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_assertion
a
np:Assertion
.
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_provenance
a
np:Provenance
.
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_assertion
{
miriam-gene:57190
a
ncit:C16612
.
lld:C0030552
a
ncit:C7057
.
dgn-gda:DGNc4115272c07207e2bb4396a494c9588f
sio:SIO_000628
miriam-gene:57190
,
lld:C0030552
;
a
sio:SIO_001122
.
}
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_provenance
{
dgn-np:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_assertion
dcterms:description
"[We sequenced SEPN1 in five unrelated CFTD patients with scoliosis and respiratory muscle weakness and screened an additional 22 CFTD patients for abnormalities in SEPN1 by Western blotting and restriction digest for the 943G-->A mutation.]. 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:16365872
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP929159.RAOUPCIBDnThO-eCQUiO2Z2TwZ1PXL8_gQp9B_nXxfcGA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:07+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}