@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q
> .
@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:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_head
{
this:
np:hasAssertion
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_assertion
;
np:hasProvenance
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_assertion
a
np:Assertion
.
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_provenance
a
np:Provenance
.
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_assertion
{
miriam-gene:2821
a
ncit:C16612
.
lld:C0001175
a
ncit:C7057
.
dgn-gda:DGNf62946bcf112f55d18c2211c3e3e3467
sio:SIO_000628
miriam-gene:2821
,
lld:C0001175
;
a
sio:SIO_001121
.
}
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_provenance
{
dgn-np:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_assertion
dcterms:description
"[In AIDS the basic defect would be the human specific inability to distinguish between the amino acid sequence of neuroleukin and peptides derived from the gp120 envelope protein of HIV, resulting in a slowly progressing failure of the CD4+ T cell-mediated immunity.]. 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:2041484
;
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:NP430883.RAp5qi7jQeb7sbO3JKdAHzB5MuI_RGuslLjhUdl8le75Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}