Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_assertion wasGeneratedBy ECO_0000203 NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_assertion wasDerivedFrom befree-20150227 NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_assertion SIO_000772 18059085 NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_assertion evidence source_evidence_literature NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.
- NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_assertion description "[Therefore, abnormalities of the POU1F1 gene are known to be responsible for a phenotype causing combined pituitary hormone deficiency (CPHD) involving growth hormone, prolactin and thyrotropin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647003.RAvZTBFphCLBv39-U8Ls2b7YxRuJDvk8g_gGpi_GKcbzw130_provenance.