http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#head
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#assertion
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#provenance
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#assertion
http://rdf.disgenet.org/resource/gda/DGN7eb7003571a8abb1cf24d659237bd2a6
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/672
http://rdf.disgenet.org/resource/gda/DGN7eb7003571a8abb1cf24d659237bd2a6
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0678222
http://rdf.disgenet.org/resource/gda/DGN7eb7003571a8abb1cf24d659237bd2a6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#provenance
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#assertion
http://purl.org/dc/terms/description
[BRCA1 and BRCA2 mutation carriers could potentially be among the first groups of individuals for whom clinically applicable risk profiling could be developed using the common breast cancer susceptibility variants identified through GWAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#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/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/21285145
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#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/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/dc/terms/created
2017-10-17T13:11:02+02:00
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP131399.RA1-JxgQk6J1T1Cu1EOuEIHkL3IiYo0SaW5dQLNAW9LRU
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