@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0
> .
@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:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_head
{
this:
np:hasAssertion
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion
;
np:hasProvenance
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance
;
np:hasPublicationInfo
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion
a
np:Assertion
.
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance
a
np:Provenance
.
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0007682
a
ncit:C7057
.
dgn-gda:DGNdf3ff2738318a6b309ecb3b752e931d4
sio:SIO_000628
miriam-gene:920
,
lld:C0007682
;
a
sio:SIO_001121
.
}
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance
{
dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion
dcterms:description
"[These results predict the presence of HIV-1 variants with increased CCR5 affinity and reduced dependence on CCR5 and CD4 in the brains of some AIDS patients with central nervous system disease and suggest that R5 variants with increased CCR5 affinity may represent a pathogenic viral phenotype contributing to the neurodegenerative manifestations of AIDS.]. 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:12021361
;
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:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}