@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM
> .
@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:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_head
{
this:
np:hasAssertion
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_assertion
;
np:hasProvenance
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_assertion
a
np:Assertion
.
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_provenance
a
np:Provenance
.
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_assertion
{
miriam-gene:4175
a
ncit:C16612
.
lld:C1857231
a
ncit:C7057
.
dgn-gda:DGNafa2f2a677bda0516c0b3126207c1975
sio:SIO_000628
miriam-gene:4175
,
lld:C1857231
;
a
sio:SIO_001121
.
}
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_provenance
{
dgn-np:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_assertion
dcterms:description
"[The aims of this study were to identify polymorphisms in the MCM6 region associated with the lactase persistence phenotype and to determine the distribution of LCT gene haplotypes in 981 individuals from North, Northeast and South Brazil.]. 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:23029545
;
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:NP875588.RA_qNL1riFNej4QPVxqdPpVm1zBzxL_1cgDKd-RoUHxRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}