@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk
> .
@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:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_head
{
this:
np:hasAssertion
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_assertion
;
np:hasProvenance
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_assertion
a
np:Assertion
.
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_provenance
a
np:Provenance
.
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0751072
a
ncit:C7057
.
dgn-gda:DGN9fac8e6c97e1639c30743ba28629a8cf
sio:SIO_000628
miriam-gene:7124
,
lld:C0751072
;
a
sio:SIO_001121
.
}
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_provenance
{
dgn-np:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_assertion
dcterms:description
"[Recent fundamental discoveries about progranulin biology, including the findings that sortilin and tumor necrosis factor receptor (TNFR) are high affinity progranulin receptors, are beginning to shed light on the mechanism(s) by which progranulin deficiency causes FTLD.]. 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:21892758
;
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:NP881538.RAP2F06BLI8V0dvmYqAB7zdaLzxym3-d5C_IC9anCuEIk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}