Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_assertion description "[The method of choice was polymerase chain reaction with sequence-specific primers (PCR-SSP) using low-resolution typing kits, with determination of the alleles class I (HLA-A, HLA-B and HLA-C) and class II (HLA-DRB1, DRB3, DRB4, DRB5 and DQB1) performed in 30 Afro-Brazilian PR-diagnosed patients and 45 healthy individuals as the control group (PR-C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_assertion evidence source_evidence_literature NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_assertion SIO_000772 16405603 NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_assertion wasDerivedFrom befree-20140225 NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_assertion wasGeneratedBy ECO_0000203 NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188849.RA3eORMHaBw3SOvjUdhgVNlLyezSKaoAHSye5orPIp-ME130_provenance.