Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion description "[Analysis of the CRELD1 gene from individuals with non-trisomy 21-associated AVSD identified heterozygous missense mutations in nearly 6% of this population, including mutations in isolated AVSD and AVSD associated with heterotaxy syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion evidence source_evidence_literature NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion SIO_000772 12632326 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion wasDerivedFrom befree-20140225 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_assertion wasGeneratedBy ECO_0000203 NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862293.RAzyrAeqPBMLTYz5aJitxTpoe3mYYI3P9UHuGifuO84Nw130_provenance.