@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg
> .
@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:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_head
{
this:
np:hasAssertion
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_assertion
;
np:hasProvenance
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_assertion
a
np:Assertion
.
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_provenance
a
np:Provenance
.
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_assertion
{
miriam-gene:2520
a
ncit:C16612
.
lld:C0038395
a
ncit:C7057
.
dgn-gda:DGN3597a0d5ec02ea3b61102ba6c54b765a
sio:SIO_000628
miriam-gene:2520
,
lld:C0038395
;
a
sio:SIO_001121
.
}
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_provenance
{
dgn-np:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_assertion
dcterms:description
"[To study the importance of CFH binding in vivo (i.e., for pathogenesis of streptococcal infections), we used our recent finding that GAS binding to CFH is diminished in vitro by polymorphism 402H, which is also associated with age-related macular degeneration.]. 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:22140259
;
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:NP203273.RAcc76byrIwVob6TWOeDePQGevHW3dljNnn2klnD5HJkg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}