@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho
> .
@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:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_head
{
this:
np:hasAssertion
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion
;
np:hasProvenance
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance
;
np:hasPublicationInfo
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion
a
np:Assertion
.
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance
a
np:Provenance
.
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion
{
miriam-gene:4254
a
ncit:C16612
.
lld:C0002874
a
ncit:C7057
.
dgn-gda:DGN073fd7edbc3f3edcb9e6cb39a6b4d1f4
sio:SIO_000628
miriam-gene:4254
,
lld:C0002874
;
a
sio:SIO_001121
.
}
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_provenance
{
dgn-np:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_assertion
dcterms:description
"[In order to investigate the levels of stem cell factor (SCF) and its receptor c-kit protein and mRNA in pediatric aplastic anemia (AA) and their relevance to the pathogenesis, immunocytochemical and in situ hybridization were utilized to detect the expression of SCF and its receptor c-kit gene protein and mRNA, respectively in 59 children with AA and 51 normal controls.]. 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:15934301
;
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:NP282532.RAxmCxaBT_PfmCSABTcs5l0bWiKKGHsbxRXZ28rop7Lho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}