Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_assertion wasGeneratedBy ECO_0000203 NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_assertion wasDerivedFrom befree-20150227 NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_assertion SIO_000772 17139695 NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_assertion evidence source_evidence_literature NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.
- NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_assertion description "[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759841.RAFm7H3agGVX4lOkm94PdqUI85nnEy6IZcF8KdNDulNwo130_provenance.