Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_assertion description "[In 1980 the clinical syndrome of X-linked hypogammaglobulinemia and isolated growth hormone deficiency (XLA/GHD) was described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_assertion evidence source_evidence_literature NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_assertion SIO_000772 7650402 NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_assertion wasDerivedFrom befree-20140225 NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_assertion wasGeneratedBy ECO_0000203 NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP688048.RApnvxXe4R1s_NpcskDVGNYhT2_eGJTStauyZov_MkkuI130_provenance.