Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion> ?p ?o ?g. }
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- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion type Assertion NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_head.
- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion wasGeneratedBy ECO_0000203 NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_provenance.
- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion wasDerivedFrom befree-20150227 NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_provenance.
- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion SIO_000772 17041934 NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_provenance.
- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion evidence source_evidence_literature NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_provenance.
- NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_assertion description "[Some clinical features in patients with this new chromosomal disorder present a substantial overlap with DG/VCFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723293.RAZKvgGxu1u9HJisHykWiUjBpz1dmTWMvZkRnlAyEvoEA130_provenance.