Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion wasGeneratedBy ECO_0000203 NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion wasDerivedFrom befree-20150227 NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion SIO_000772 10822217 NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion evidence source_evidence_literature NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.
- NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_assertion description "[FGHD due to an autosomal recessive GHRH-R gene mutation leads to marked dwarfism, phenotypically and hormonally indistinguishable from other forms of isolated GH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424992.RA0QA4m9OHwzuKO0vbZl9kFm_HIrllSZLPqfxATsYYbtQ130_provenance.