Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_assertion wasGeneratedBy ECO_0000203 NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_assertion wasDerivedFrom befree-20150227 NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_assertion SIO_000772 25056248 NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_assertion evidence source_evidence_literature NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.
- NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_assertion description "[In particular, a patient with a severe bilateral Madelung deformity without short stature showed a homozygous alteration identical to the recently described 47.5 kb PAR1 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390067.RA-i3pA7Y3XKhl2tf9k5EPUsOPAa274DMw7ZD1Yx1HaNc130_provenance.