@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo
> .
@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:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_head
{
this:
np:hasAssertion
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_assertion
;
np:hasProvenance
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_provenance
;
np:hasPublicationInfo
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_assertion
a
np:Assertion
.
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_provenance
a
np:Provenance
.
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_assertion
{
miriam-gene:929
a
ncit:C16612
.
lld:C0334663
a
ncit:C7057
.
dgn-gda:DGNeb781dea03630fe21d879e72c6ddd818
sio:SIO_000628
miriam-gene:929
,
lld:C0334663
;
a
sio:SIO_001121
.
}
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_provenance
{
dgn-np:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_assertion
dcterms:description
"[The expression of circulating monocyte markers in malignant histiocytosis suggests that this tumor originates in monocytes or free histiocytes, whereas the phenotype of true histiocytic lymphoma is compatible with an origin in fixed histiocytes, which generally are devoid of the monocyte markers CD11b and CD14.]. 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:1647137
;
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:NP295666.RAekCRNfDPF8_eNr8Co3C47_V73HqWV32-0RBTA4RpoMo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}