@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0
> .
@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:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_head
{
this:
np:hasAssertion
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_assertion
;
np:hasProvenance
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_provenance
;
np:hasPublicationInfo
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_assertion
a
np:Assertion
.
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_provenance
a
np:Provenance
.
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_assertion
{
miriam-gene:2525
a
ncit:C16612
.
lld:C0577631
a
ncit:C7057
.
dgn-gda:DGNdf7513428905cc92cc91c371b5a41e8a
sio:SIO_000628
miriam-gene:2525
,
lld:C0577631
;
a
sio:SIO_001122
.
}
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_provenance
{
dgn-np:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_assertion
dcterms:description
"[Four specific SNPs of the Lewis genotype are common in the population at large. However, these four SNPs seem to fail to explain the majority of Lewis-negative phenotype in African Americans, given that Lewis-negative genotype prevalence was about one-third of what was expected. Use of rapid DNA sequencing and simultaneous Lewis phenotype determination could avoid the problems associated with haplotype determination and Lewis genotype grouping. Further studies testing SNPs of the Lewisgene are warranted, in particular among African Americans.]. 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:12424536
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43851.RA3xT4j5o9RuNeuuPhy2C_gGQGvT6WqGGNpinmvJPZAl0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}