@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_head
{
this:
np:hasAssertion
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_assertion
;
np:hasProvenance
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_provenance
;
np:hasPublicationInfo
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_assertion
a
np:Assertion
.
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_provenance
a
np:Provenance
.
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_assertion
{
miriam-gene:51119
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNbeadbc77aa3d7ba3ccfe7c713a60d837
sio:SIO_000628
miriam-gene:51119
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_provenance
{
dgn-np:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_assertion
dcterms:description
"[We have studied both by isoelectric focusing and polyacrylamide gel electrophoresis in the presence of SDS, sera of individuals homozygous (25) and heterozygous (26) for cystic fibrosis and compared them to controls (13).]. 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:2440620
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP440125.RA6RmSOql9t7elVICyWFQ2jiZ-zd9QvmesC5HJ1iX9TVE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}