Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_assertion description "[Cohen recently described a syndrome that includes both of these defects, which he called `craniofrontonasal dysplasia.` We report a three-generation family in which five individuals (four females, one male) have varying degrees of frontonasal dysplasia and craniosynostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_assertion evidence source_evidence_literature NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_assertion SIO_000772 7166597 NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_assertion wasDerivedFrom befree-20140225 NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_assertion wasGeneratedBy ECO_0000203 NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478720.RAdwn25qTfRcx6-_MOu1Lwne78gSMyWKUdI3NDwcFm9Gg130_provenance.