@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4
> .
@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:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_head
{
this:
np:hasAssertion
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_assertion
;
np:hasProvenance
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_assertion
a
np:Assertion
.
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_provenance
a
np:Provenance
.
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_assertion
{
miriam-gene:4842
a
ncit:C16612
.
lld:C1867403
a
ncit:C7057
.
dgn-gda:DGN3590aa0cc5af7c1d3ef32a0eb6da32e1
sio:SIO_000628
miriam-gene:4842
,
lld:C1867403
;
a
sio:SIO_001121
.
}
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_provenance
{
dgn-np:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_assertion
dcterms:description
"[The etiological role of the gene for neuronal nitric oxide synthase (NOS1) in infantile pyloric stenosis (PS) was investigated by analysis of two intragenic polymorphisms (NOS1a and NOS1b) in 27 families.]. 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:8571963
;
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:NP415900.RAbtIFWnhuxAqRZoc2_a2bflhigtWv4e_0f1XelQEMzQ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}