Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion description "[Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion evidence source_evidence_literature NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion SIO_000772 23615299 NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion wasDerivedFrom befree-2016 NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_assertion wasGeneratedBy ECO_0000203 NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1072019.RAxDXsbyU2OGH_U14r0-4LuU6WYBHn3Y4fhJ-OWlCQvTc130_provenance.