@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8
> .
@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:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_head
{
this:
np:hasAssertion
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_assertion
;
np:hasProvenance
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_provenance
;
np:hasPublicationInfo
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_assertion
a
np:Assertion
.
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_provenance
a
np:Provenance
.
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_assertion
{
miriam-gene:5905
a
ncit:C16612
.
lld:C0027126
a
ncit:C7057
.
dgn-gda:DGNa6052dee3c46236ee5385ae62921a940
sio:SIO_000628
miriam-gene:5905
,
lld:C0027126
;
a
sio:SIO_001121
.
}
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_provenance
{
dgn-np:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_assertion
dcterms:description
"[The concept of segregation distortion, where there is preferential transmission of the larger allele at the DM locus, has been put forward to explain partially the maintenance of DM in the population.]. 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:9863607
;
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:NP330276.RAyFriembJ1vBY86A0xMO8g0DYLgT-XyyjnS4SuVc95P8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}