Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_assertion wasGeneratedBy ECO_0000203 NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_assertion wasDerivedFrom befree-20140225 NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_assertion SIO_000772 18554282 NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_assertion evidence source_evidence_literature NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_assertion description "[Mandibuloacral dysplasia type A (MADA; OMIM 248370), a rare disorder caused by mutation in the LMNA gene, is characterized by post-natal growth retardation, craniofacial and skeletal anomalies (mandibular and clavicular hypoplasia, acroosteolysis, delayed closure of cranial sutures, low bone mass and joint contractures), cutaneous changes and partial lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP701261.RA7R2ZJyh3wQ9cy42rjwGUPLRqTX_BWF1t4Yt7ivvAh7s130_provenance.