@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw
> .
@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:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_head
{
this:
np:hasAssertion
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_assertion
;
np:hasProvenance
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_provenance
;
np:hasPublicationInfo
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_assertion
a
np:Assertion
.
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_provenance
a
np:Provenance
.
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_assertion
{
miriam-gene:2212
a
ncit:C16612
.
lld:C0024301
a
ncit:C7057
.
dgn-gda:DGN643f0c599b8cc08156e2fd237b74869b
sio:SIO_000628
miriam-gene:2212
,
lld:C0024301
;
a
sio:SIO_001121
.
}
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_provenance
{
dgn-np:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_assertion
dcterms:description
"[The prognostic role of FCGR3A and FCGR2A polymorphisms in patients with follicular lymphoma treated with rituximab and chemotherapy combination remains controversial and has not been evaluated in the context of rituximab maintenance.]. 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:22885164
;
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:NP770787.RAHd7YVnHPzRQYm-txpWmauPwTfFNS0zinPQM7mREgEyw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}