@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA
> .
@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:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_head
{
this:
np:hasAssertion
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_assertion
;
np:hasProvenance
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_provenance
;
np:hasPublicationInfo
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_assertion
a
np:Assertion
.
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_provenance
a
np:Provenance
.
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0085762
a
ncit:C7057
.
dgn-gda:DGN6e6e3e7dc0c971c7ac88f08b9432a6e8
sio:SIO_000628
miriam-gene:3077
,
lld:C0085762
;
a
sio:SIO_001121
.
}
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_provenance
{
dgn-np:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_assertion
dcterms:description
"[These patients differed from patients without PCT in that they were men, past history of alcohol abuse and HFE gene mutations were more common and the source of infection was almost always unknown.]. 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:12737448
;
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:NP866187.RAHXsTTTrq7G7VaryQjVvsN5G_csejVLCnzDL-Nm6a1HA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:49+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" .
}