@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY
> .
@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:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_head
{
this:
np:hasAssertion
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_assertion
;
np:hasProvenance
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_provenance
;
np:hasPublicationInfo
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_assertion
a
np:Assertion
.
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_provenance
a
np:Provenance
.
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_assertion
{
miriam-gene:4179
a
ncit:C16612
.
lld:C0013146
a
ncit:C7057
.
dgn-gda:DGNd1b64abe872285aaae730f68643f7038
sio:SIO_000628
miriam-gene:4179
,
lld:C0013146
;
a
sio:SIO_001121
.
}
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_provenance
{
dgn-np:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_assertion
dcterms:description
"[Specifically, this latter function of CD46 is a tantalizing discovery - it may not only have delivered the explanation as to why so many pathogens use and abuse CD46 as cell entry receptor but clearly has important clinical implications for the better understanding of Th1-mediated disease states and novel therapeutic approaches for their amelioration.]. 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:21488871
;
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:NP832629.RADqFnm2NKoxRDei1I7-VXoel5sh7K0KRzlmGBRH-71UY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}