@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s
> .
@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:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_head
{
this:
np:hasAssertion
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_assertion
;
np:hasProvenance
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_provenance
;
np:hasPublicationInfo
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_assertion
a
np:Assertion
.
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_provenance
a
np:Provenance
.
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN5204c712781ba9c8fd99ce6a3bc71d5b
sio:SIO_000628
miriam-gene:2100
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_provenance
{
dgn-np:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_assertion
dcterms:description
"[These results suggest that endogenous estrogen and genetic variations in ESR2 may individually, or more likely jointly, affect CRC risk in male Han Chinese population, while larger studies are needed to validate our findings.]. 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:22759347
;
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:NP377782.RA2m4sh9UJiFBt2htPkPLisztIAOnqbRl4ICu_CMmRS8s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}