@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE
> .
@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:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_head
{
this:
np:hasAssertion
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_assertion
;
np:hasProvenance
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_assertion
a
np:Assertion
.
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_provenance
a
np:Provenance
.
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_assertion
{
miriam-gene:30811
a
ncit:C16612
.
lld:C0020305
a
ncit:C7057
.
dgn-gda:DGN1e0e1d8d654eeff366ba4afdc848b63c
sio:SIO_000628
miriam-gene:30811
,
lld:C0020305
;
a
sio:SIO_001121
.
}
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_provenance
{
dgn-np:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_assertion
dcterms:description
"[The human parvovirus B19 (PVB19), an erythrovirus causing diverse clinical manifestations ranging from asymptomatic or mild to more severe outcomes such as hydrops fetalis, is the only currently known human pathogenic parvovirus.]. 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:16329659
;
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:NP335187.RALjMcsLlKa0t_MyhBEkdZbbol_RCnC5X_jJD9g_FieCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}