@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM
> .
@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:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_head
{
this:
np:hasAssertion
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_assertion
;
np:hasProvenance
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_assertion
a
np:Assertion
.
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_provenance
a
np:Provenance
.
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_assertion
{
miriam-gene:8795
a
ncit:C16612
.
lld:C0036631
a
ncit:C7057
.
dgn-gda:DGNf461ba2f936b1e6fa7c8fd64d833032a
sio:SIO_000628
miriam-gene:8795
,
lld:C0036631
;
a
sio:SIO_001121
.
}
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_provenance
{
dgn-np:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_assertion
dcterms:description
"[Increases were noted in the frequencies of Aw33, B5, DR5, and DRw6 among the patients with pure seminoma, A3 and B7 among the patients with embryonal carcinoma with or without seminoma, and Aw32 among the patients with yolk sac tumor components.]. 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:6280859
;
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:NP778063.RAOexAGU50kkUJp2ZA_erjv4ywaEO8s2iysbW6jGobLDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}