@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_assertion
a
np:Assertion
.
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_provenance
a
np:Provenance
.
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4312
a
ncit:C16612
.
lld:C0027092
a
ncit:C7057
.
dgn-gda:DGNcaf0713e836ca964e9a7ce17f14c7103
sio:SIO_000628
miriam-gene:4312
,
lld:C0027092
;
a
sio:SIO_001122
.
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dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_provenance
{
dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_assertion
dcterms:description
"[Statistically significant genetic associations of ocular refraction to polymorphisms near MMP1 and within MMP2 were identified in the AMISH but not among the ASHK families. The results suggest that the MMP1 and MMP2 genes are involved in refractive variat]. 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:20484597
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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 .
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dgn-np:NP176532.RA0ROcwpXn4GWETOARVQWesksUcPZj-ZwiCSOPLaDqo_A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:07+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
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