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- source_evidence_literature type ECO_0000212 NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_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." NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_assertion evidence source_evidence_literature NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_assertion SIO_000772 23638902 NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_assertion wasDerivedFrom befree-2016 NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_assertion wasGeneratedBy ECO_0000203 NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074470.RAGOIFxr-tac-Dbr7xUKs-MuPmkj7Dfelk3bMAZ8FKnDU130_provenance.