@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA
> .
@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:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_head
{
this:
np:hasAssertion
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_assertion
;
np:hasProvenance
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_provenance
;
np:hasPublicationInfo
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_assertion
a
np:Assertion
.
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_provenance
a
np:Provenance
.
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNa21951d95b28249a2f3f962687f9942c
sio:SIO_000628
miriam-gene:213
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_provenance
{
dgn-np:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_assertion
dcterms:description
"[Although the level of albumin is altered in children with CF, the gene does not segregate with CF, and therefore albumin can be excluded as the site of the basic defect.]. 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:2984105
;
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:NP723304.RAkQ9OAROXEzRzLCcA-QdNR0dkp2BLezLmnEoOKbWuaVA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}