Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_assertion description "[To clarify the role of HEY2 in human CHD and AGS, we screened by direct sequencing 23 children with CHD and 38 patients diagnosed with AGS, which lack mutations in the JAG1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_assertion evidence source_evidence_literature NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_assertion SIO_000772 15389319 NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_assertion wasDerivedFrom befree-20140225 NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_assertion wasGeneratedBy ECO_0000203 NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP459903.RAEriBdCldDaGO-7JVBzXTYTLG1_4ADU28qJ_ow199-CU130_provenance.