Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_assertion description "[About 30% of the mutations causing nonsyndromic X-linked mental retardation (MRX) are thought to be located in Xp11 and in the pericentromeric region, with a particular clustering of gene defects in a 7.4 Mb interval flanked by the genes ELK1 and ALAS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_assertion evidence source_evidence_literature NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_assertion SIO_000772 16969374 NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_assertion wasDerivedFrom befree-20150227 NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_assertion wasGeneratedBy ECO_0000203 NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872496.RAid7nk_d8i_R3dXpQ3FV8Byh3znzCzybcOjch5wnxgeI130_provenance.