Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion description "[A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion evidence source_evidence_literature NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion SIO_000772 21271662 NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion wasDerivedFrom befree-20140225 NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_assertion wasGeneratedBy ECO_0000203 NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP841355.RA6QiNWm2HBhFWTeKW_ADJB_p4Id2FSJ71cphwH7DA1Bk130_provenance.