@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI
> .
@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:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_head
{
this:
np:hasAssertion
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_assertion
;
np:hasProvenance
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_assertion
a
np:Assertion
.
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_provenance
a
np:Provenance
.
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_assertion
{
miriam-gene:720
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGN55b389834a31fe21ba750e78f7474ef7
sio:SIO_000628
miriam-gene:720
,
lld:C0017661
;
a
sio:SIO_001121
.
}
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_provenance
{
dgn-np:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_assertion
dcterms:description
"[In addition, no significant differences in C4A and C4B allelic frequencies were observed in comparisons of pediatric patients (diagnostic biopsy before age 18 years) and adult patients with IgA nephropathy in either U.S. population.]. 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:2329414
;
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:NP249088.RAmdJmgJd8eulOMxgaoLYIIa8m3TXMYMVj3Gc98fHEWNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}