@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8
> .
@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:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_head
{
this:
np:hasAssertion
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion
;
np:hasProvenance
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion
a
np:Assertion
.
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance
a
np:Provenance
.
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion
{
miriam-gene:6288
a
ncit:C16612
.
lld:C1838022
a
ncit:C7057
.
dgn-gda:DGN2dcac168532e1ff2cf708d014de286be
sio:SIO_000628
miriam-gene:6288
,
lld:C1838022
;
a
sio:SIO_001121
.
}
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_provenance
{
dgn-np:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_assertion
dcterms:description
"[A significant difference in the frequency of the A1 allele was found among these three groups of boys, with the SAA group having the highest A1 allele frequency (.313), followed by the SRA (.139) and the SSD (.133) groups.]. 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:8128963
;
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:NP786007.RA9O5l8AMxTVLpxcvY7v2NgLJE0ujjR-Q8U6lW4Z_6rV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}