Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion evidence source_evidence_literature NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion SIO_000772 23063620 NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion wasDerivedFrom befree-20150227 NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_assertion wasGeneratedBy ECO_0000203 NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP368255.RAUiKorlx3QqfKVOEz2_rBEhXre52y_7oFW41iMM3oCCg130_provenance.