http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#head
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#provenance
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://rdf.disgenet.org/resource/gda/DGNa58f6e3da127a4b4b6f4a895f4461fbd
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1080
http://rdf.disgenet.org/resource/gda/DGNa58f6e3da127a4b4b6f4a895f4461fbd
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0028960
http://rdf.disgenet.org/resource/gda/DGNa58f6e3da127a4b4b6f4a895f4461fbd
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#provenance
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://purl.org/dc/terms/description
[We screened 80 men with idiopathic azoospermia, 50 men with severe oligozoospermia, 70 men with oligoasthenoteratozoospermia, and 7 men with congenital bilateral absence of the vas deferens (CBAVD), as well as 95 controls from Slovenia, for mutations in 10 CFTR exons that include the majority of the most common cystic fibrosis (CF) disease causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#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/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/11788091
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/GAD
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/GAD
http://purl.org/pav/importedOn
2017-02-21
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/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/dc/terms/created
2017-10-17T13:11:31+02:00
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP208921.RAiJaahHPuFDE5i2bkRKGI29fLAUYlrwz0Y9LKhUffKTY
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