Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_assertion description "[Here, we report two familial cases of LWD with a large Xp terminal deletion (approximately 943 kb) of distal PAR1 encompassing the SHOX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_assertion evidence source_evidence_literature NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_assertion SIO_000772 19400538 NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_assertion wasDerivedFrom befree-20140225 NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_assertion wasGeneratedBy ECO_0000203 NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP841407.RAmeIwEX0hWG7gazaIw_ZKSL1MvUV1a-VIxikrDFMpG0A130_provenance.