Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_assertion description "[Due to tight linkage between the HH locus and the HLA-A locus, 172 relatives of the 29 unrelated probands could be assigned into three groups: G0 who were considered to be normal (n = 53), G1 who were considered to be heterozygotes (n = 105), and G2 who were considered to be homozygotes (n = 14), according to whether they had no, one or two HLA haplotypes in common with the proband.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_assertion evidence source_evidence_literature NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_assertion SIO_000772 7924465 NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_assertion wasDerivedFrom befree-20140225 NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_assertion wasGeneratedBy ECO_0000203 NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401555.RA7XrTt6owC4YPbaDgaSVOohkvD_QMrSRheJWIVawsnqg130_provenance.