@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk
> .
@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:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_head
{
this:
np:hasAssertion
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_assertion
;
np:hasProvenance
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_provenance
;
np:hasPublicationInfo
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_assertion
a
np:Assertion
.
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_provenance
a
np:Provenance
.
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_assertion
{
miriam-gene:4597
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN2ec63a8122ae662f03f59c6413032240
sio:SIO_000628
miriam-gene:4597
,
lld:C0028326
;
a
sio:SIO_001121
.
}
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_provenance
{
dgn-np:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_assertion
dcterms:description
"[This supports the need to characterize the spectrum of hematologic abnormalities in individuals with NS and to better define the impact of the PTPN11 lesion on the disease course in patients with NS/MPD and JMML.]. 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:15928039
;
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:NP338976.RAn4bhcfe3jWN0c34F_bav5rWPwXdBZby64gx_PSs8Vtk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}