Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP370624.RAmfIWYVnxD1wrITD3c72jWhx2j57bnjoiS-2mBHBkLxU130_provenance.