Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion> ?p ?o ?g. }
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- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion type Assertion NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_head.
- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion description "[TTD is a rare autosomal recessive multisystem disorder associated, in many patients, with a defect in nucleotide-excision repair; but in contrast to XP patients, TTD patients are not cancer prone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion evidence source_evidence_literature NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion SIO_000772 9758621 NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion wasDerivedFrom befree-20140225 NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_assertion wasGeneratedBy ECO_0000203 NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.