@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24
> .
@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:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_head
{
this:
np:hasAssertion
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_assertion
;
np:hasProvenance
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_provenance
;
np:hasPublicationInfo
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_assertion
a
np:Assertion
.
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_provenance
a
np:Provenance
.
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0007789
a
ncit:C7057
.
dgn-gda:DGN952ceaa8a592a768e5102c4bef5f6402
sio:SIO_000628
miriam-gene:4153
,
lld:C0007789
;
a
sio:SIO_001122
.
}
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_provenance
{
dgn-np:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_assertion
dcterms:description
"[Mannose-binding lectin (MBL) haplotypes with intermediate and high levels of circulating MBL may be associated with an increased risk of cerebral palsy in the presence of exposure to viral infection and may act as susceptibility factors for CP ]. 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:18455525
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP146645.RA-GXW_u3f-MTuFodchuH_uWr_r3szqXam6b1719uKb24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:16+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" .
}