@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA
> .
@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:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_head
{
this:
np:hasAssertion
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_assertion
;
np:hasProvenance
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_provenance
;
np:hasPublicationInfo
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_assertion
a
np:Assertion
.
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_provenance
a
np:Provenance
.
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_assertion
{
miriam-gene:6343
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGNb6cf396139cd9d2c43922c706be15c48
sio:SIO_000628
miriam-gene:6343
,
lld:C0018133
;
a
sio:SIO_001121
.
}
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_provenance
{
dgn-np:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_assertion
dcterms:description
"[Treatment or prophylaxis of invasive fungal infection in recipients of haemopoietic SCT (HSCT) may require management of coexistent malnutrition, organ dysfunction and GVHD, all of which create added potential for inter- and intra-patient variations in drug metabolism as well as drug interactions.]. 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:21785468
;
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:NP415719.RAFQNwPbCmsBRPA5V53rRfwz_ZMOu7UNGpPGZN__ioElA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}