@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE
> .
@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:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_head
{
this:
np:hasAssertion
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_assertion
;
np:hasProvenance
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_provenance
;
np:hasPublicationInfo
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_assertion
a
np:Assertion
.
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_provenance
a
np:Provenance
.
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_assertion
{
miriam-gene:718
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN8ccc99073258c86ee2c6d128d247e635
sio:SIO_000628
miriam-gene:718
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_provenance
{
dgn-np:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_assertion
dcterms:description
"[Only S and F alleles of C3 ( C3S and C3F) were recognized and C3F frequencies were 0.33 in Crohn patients with small bowel disease, 0.23 in all Crohn patients, 0.18 in ulcerative colitis patients and 0.17 in healthy volunteers.]. 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:6731047
;
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:NP577761.RA4VjRZ65C2Z3sTzxbWOvOtgXJRGqoryQrFzKtd3a4XkE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+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" .
}