Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_assertion description "[While genetic risk factors still remain largely unknown, human leukocyte antigen (HLA) genes have been a focus of attention since the discovery of an HLA association with NPC in 1973 and, two years later, that NPC susceptibility in highest-risk Cantonese involved the co-occurrence of multi-HLA locus combinations of HLA genes as chromosome combinations, or haplotypes (e.g.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_assertion evidence source_evidence_literature NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_assertion SIO_000772 21272439 NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_assertion wasDerivedFrom befree-20140225 NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_assertion wasGeneratedBy ECO_0000203 NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP323022.RAP8xy52fmWjLc7D6jAkDrdiHPA7FhRQQq5Yp0BQBQfPI130_provenance.