Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_assertion description "[A binding partner of Upf3b, RBM8a, is located in the 1q21.1 copy-number variation (CNV) associated with mental retardation, autism [4], schizophrenia [5], and microcephaly [6].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_assertion evidence source_evidence_literature NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_assertion SIO_000772 23638902 NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_assertion wasDerivedFrom befree-20150227 NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_assertion wasGeneratedBy ECO_0000203 NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.
- befree-20150227 importedOn "2015-02-27" NP941091.RAFW2WeROhUjhE84q0qsi9VbFXjJ3j5hfGg_ohhNts4Is130_provenance.