Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion> ?p ?o ?g. }
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- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion type Assertion NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_head.
- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion description "[In addition, in a family affected by dominantly inherited early-onset osteoporosis, a heterozygous WNT1 missense mutation was identified in affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_provenance.
- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion evidence source_evidence_curated NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_provenance.
- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion SIO_000772 23499309 NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_provenance.
- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion wasDerivedFrom uniprot-2016 NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_provenance.
- NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_assertion wasGeneratedBy ECO_0000218 NP7403.RAaFmEClrKWRR6UzWw8Pf02RU5WvHYmJV-XwcXarqqUts130_provenance.