Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion> ?p ?o ?g. }
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- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion type Assertion NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_head.
- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion wasGeneratedBy ECO_0000218 NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_provenance.
- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion wasDerivedFrom uniprot-2016 NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_provenance.
- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion SIO_000772 11968094 NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_provenance.
- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion evidence source_evidence_curated NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_provenance.
- NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_assertion description "[A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1988.RAm4I7u4CPMMxyo2GrqCwdw4-fDX0SwZtHCXHQTPu87dk130_provenance.