Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_assertion description "[Several sets of allele level haplotypes that could not be discriminated by routine HLA-A, -B, and -DRB1 low-resolution typing originated from allelic diversity of A2, B61, DR4, and DR8 serologic groups. Information obtained in this study will be useful fo]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_assertion evidence source_evidence_literature NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_assertion SIO_000772 15853898 NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_assertion wasDerivedFrom gad-20150221 NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_assertion wasGeneratedBy ECO_0000203 NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92172.RAkpd8XNq1fp9eDzZDXFUS_SQ5Je_LyAbPnhqka-d4MS0130_provenance.