@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74
> .
@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/
> .
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_head
{
this:
np:hasAssertion
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_assertion
a
np:Assertion
.
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_provenance
a
np:Provenance
.
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_assertion
{
miriam-gene:4157
a
ncit:C16612
.
lld:C1849452
a
ncit:C7057
.
dgn-gda:DGN199ca7ab56cf48a8b0adfe43595dd5de
sio:SIO_000628
miriam-gene:4157
,
lld:C1849452
;
a
sio:SIO_001122
.
}
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_provenance
{
dgn-np:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_assertion
dcterms:description
"[Three single nucleotide polymorphisms (rs28777, rs35391, and rs16891982) in the MATP gene (SLC45A2) exhibited the strongest crude association with risk, but this was attenuated to approximately the same effect size as that of a MC1R red hair color allele by controlling for ancestry of cases and controls.]. 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:19710684
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP759777.RAD7ayFEiLcCoe8n1p-mxeN8--qAa1ANERjbV3PCgSi74130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:29+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}