Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion> ?p ?o ?g. }
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- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion type Assertion NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_head.
- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion description "[Complete deficiency of the extracellular matrix glycoprotein tenascin-X (TNX) leads to recessive forms of Ehlers-Danlos syndrome, clinically characterized by hyperextensible skin, easy bruising and joint hypermobility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_provenance.
- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion evidence source_evidence_literature NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_provenance.
- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion SIO_000772 23768946 NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_provenance.
- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion wasDerivedFrom befree-20150227 NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_provenance.
- NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_assertion wasGeneratedBy ECO_0000203 NP748873.RA1M5yWVEGrAoCUAqf5Hk-VM8rhSi1xnSXJuGbsKNEsYU130_provenance.