Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_assertion description "[All samples were first screened for TWIST1 and FGFR3 mutation hot spots, and the negative samples were subsequently screened for FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_assertion evidence source_evidence_literature NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_assertion SIO_000772 22544111 NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_assertion wasDerivedFrom befree-20140225 NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_assertion wasGeneratedBy ECO_0000203 NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP770891.RA9NXA0o6_0LHBNDKn2OT4ZrI-n3tIvqDly95lBBfA3VY130_provenance.