@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_head
{
this:
np:hasAssertion
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion
;
np:hasProvenance
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance
;
np:hasPublicationInfo
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion
a
np:Assertion
.
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance
a
np:Provenance
.
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion
{
miriam-gene:3704
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGNe714ef25d73bf57e1792880b022e8eee
sio:SIO_000628
miriam-gene:3704
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance
{
dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion
dcterms:description
"[We hypothesize that patients (63%) being homozygous for both major alleles, leading to normal ITPase activity, may benefit more from the addition of ribavirin to present and future treatment regimens for HCV in spite of concomitant increased risk of anemia.]. 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:24519039
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:46+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}