@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI
> .
@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:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_head
{
this:
np:hasAssertion
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion
;
np:hasProvenance
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance
;
np:hasPublicationInfo
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion
a
np:Assertion
.
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance
a
np:Provenance
.
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0151526
a
ncit:C7057
.
dgn-gda:DGN70c8e6703e8de57097e07b5be1d3e16a
sio:SIO_000628
miriam-gene:4153
,
lld:C0151526
;
a
sio:SIO_001122
.
}
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_provenance
{
dgn-np:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_assertion
dcterms:description
"[Our data add to the knowledge about genetic predisposition to prematurity and suggest that the fetal MBL2 genotype might be an additional genetic factor contributing to the risk of premature delivery.]. 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:16912583
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP85839.RAWUaxG865TUtIWzfp-hKrgogxKnVr3gmNqnHHs2LEfWI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}