http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#head
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#provenance
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://rdf.disgenet.org/resource/gda/DGN4aa21f17ca6fe1e25530855569dca22b
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/116519
http://rdf.disgenet.org/resource/gda/DGN4aa21f17ca6fe1e25530855569dca22b
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0010068
http://rdf.disgenet.org/resource/gda/DGN4aa21f17ca6fe1e25530855569dca22b
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#provenance
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://purl.org/dc/terms/description
[Furthermore, identification of rare loss-of-function variants in genes such as PCSK9, NPC1L1, APOC3 and APOA5, which cause a markedly decreased risk of CHD and no adverse side effects, illustrates the power of translating genetic findings into novel mechanistic information and provides some optimism for the future of developing novel drugs, given the many genes associated with CHD in GWASs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/26477595
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/dc/terms/created
2017-10-17T13:19:04+02:00
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1398429.RAhk6WBOA1A_A3NlpYMzrdx_mVaCR03jmyuiWwlgqXgEE
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0