@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70
> .
@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:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_head
{
this:
np:hasAssertion
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_assertion
;
np:hasProvenance
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_provenance
;
np:hasPublicationInfo
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_assertion
a
np:Assertion
.
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_provenance
a
np:Provenance
.
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0032461
a
ncit:C7057
.
dgn-gda:DGNeb45685ba92ddb149836efbad6c37b96
sio:SIO_000628
miriam-gene:2056
,
lld:C0032461
;
a
sio:SIO_001121
.
}
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_provenance
{
dgn-np:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_assertion
dcterms:description
"[Therefore, PFCP will also be discussed here, while other congenital polycythemic states such as the Chuvash polycythemia that have elevated or inappropriately normal Epo levels will be omitted from this review in view of their distinct phenotype and unique laboratory features.]. 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:16210040
;
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:NP238327.RAz9OAuR2i64z3yWKawvOzfFfd5H6zRgWK1rXGEgRDu70130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}