@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU
> .
@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:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_head
{
this:
np:hasAssertion
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_assertion
;
np:hasProvenance
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_assertion
a
np:Assertion
.
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_provenance
a
np:Provenance
.
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_assertion
{
miriam-gene:7037
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNd71cc5aa29aeddb5015842994f585a10
sio:SIO_000628
miriam-gene:7037
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_provenance
{
dgn-np:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_assertion
dcterms:description
"[Whereas a recent study reported an increased risk of colorectal cancer associated with any HFE germ line mutation (C282Y or H63D), other investigators have concluded there is no increased risk, or that any increase is dependent on polymorphisms in HFE-interacting genes such as the transferrin receptor (TFR).]. 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:15941956
;
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:NP783318.RAALiTNaei6kWlx25pmIes2s0ksWAlceiH9eJywk77KFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}