@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ
> .
@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:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_head
{
this:
np:hasAssertion
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion
;
np:hasProvenance
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion
a
np:Assertion
.
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance
a
np:Provenance
.
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0007099
a
ncit:C7057
.
dgn-gda:DGN1786ce36d8746002930bfc786aa38ef2
sio:SIO_000628
miriam-gene:920
,
lld:C0007099
;
a
sio:SIO_001121
.
}
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance
{
dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion
dcterms:description
"[After adjustment for anal cytological diagnoses at study entry, HIV status and CD4 count, and detection of HPV types other than type 16, men with HPV16 NPL variants were 3.2 times (95% confidence interval, 1.0-10.3) more likely to develop anal CIS than were those with PL variants.]. 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:9731493
;
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:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}