@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM
> .
@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:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_head
{
this:
np:hasAssertion
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_assertion
;
np:hasProvenance
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_provenance
;
np:hasPublicationInfo
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_assertion
a
np:Assertion
.
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_provenance
a
np:Provenance
.
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_assertion
{
miriam-gene:51365
a
ncit:C16612
.
lld:C1843463
a
ncit:C7057
.
dgn-gda:DGNa9227cd961b6eb1dd6f29a0bbdfa70ea
sio:SIO_000628
miriam-gene:51365
,
lld:C1843463
;
a
sio:SIO_001121
.
}
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_provenance
{
dgn-np:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_assertion
dcterms:description
"[In patients and controls, we show that allelic expression imbalance (AEI) can be readily detected in RNA extracted from whole blood from patients carrying mutations expected to elicit NMD using mass spectrometry.]. 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:20860725
;
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:NP337822.RAwIZ6kEmZyfTxd-xExqGMsXApuB_sH-Gb_b_SIE-f4NM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}