Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_assertion description "[Deletions and point mutations of the growth hormone (GH) receptor gene (GHR) have been identified in patients with Laron syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_assertion evidence source_evidence_literature NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_assertion SIO_000772 9290257 NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_assertion wasDerivedFrom befree-20140225 NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_assertion wasGeneratedBy ECO_0000203 NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP221139.RAawxlh201sit0FHCGkthxOOAdNpeOCye_N_6ZX3EiZvA130_provenance.