Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_assertion description "[Comparison of these data with the available genetic and physical maps of 17p12 --> p11 shows that this region, which is frequently subject to rearrangement-inducing diseases, such as Smith-Magenis syndrome, Charcot-Marie-Tooth type 1A, and HNPP, presents recombination hot spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_assertion evidence source_evidence_literature NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_assertion SIO_000772 8565626 NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_assertion wasDerivedFrom befree-20140225 NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_assertion wasGeneratedBy ECO_0000203 NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP374593.RAIv1O5l64fOFuY0MRkMf60zQHDSDbF1XPfzlg2WnB9MM130_provenance.