Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_assertion description "[In addition to craniosynostosis with crouzonoid facies and acanthosis nigricans (present in all patients), melanocytic nevi, choanal atresia or stenosis, hydrocephalus, Chiari malformations and oral abnormalities were observed in the majority of the 35 patients analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_assertion evidence source_evidence_literature NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_assertion SIO_000772 17935505 NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_assertion wasDerivedFrom befree-20140225 NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_assertion wasGeneratedBy ECO_0000203 NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP602783.RA3k1vC1i50vmf7gI0u-GifpCVG-FjoyfkAH4i7cCuFIs130_provenance.