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http://rdf.disgenet.org/nanopublications.trig#NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_head
{
this:
np:hasAssertion
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion
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np:Nanopublication
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a
np:Assertion
.
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_provenance
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np:Provenance
.
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_publicationInfo
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{
miriam-gene:2064
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGNb3e1ce261fc8b547e6f3674df5b2af52
sio:SIO_000628
miriam-gene:2064
,
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;
a
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.
}
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_provenance
{
dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_assertion
dcterms:description
"[These data suggest that this SNP has variable frequency in different ethnic groups. In addition, intraracial differences in allele frequency were seen. The presence of the Val allele in the African-American population, but not in the African population is consistent with the genetic mixing, which has been identified through historical and molecular analysis. However, the presence of many first-generation immigrant populations in the United States provides warning for the overinterpretation of results from any one ethnic group. Therefore, the usefulness of the HER2 SNP in the determination of risk, prognosis, and treatment response of breast cancer will be dramatically different between ethnic populations.]. 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:11106692
;
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 .
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dgn-np:NP45006.RATPkCZIkPu9hihC4WHRE84-0WVNGlxkFP1WH62ujeQbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
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pav:createdBy
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