Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- befree-2016 importedOn "2016-02-19" NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_assertion wasGeneratedBy ECO_0000203 NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_assertion wasDerivedFrom befree-2016 NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_assertion SIO_000772 22310223 NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_assertion evidence source_evidence_literature NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.
- NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958977.RA-rT4nTBIH6zDxn8EOeRQBOV5XFOAJ0u8r5NIT4FY-xA130_provenance.