Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_assertion description "[Except for FVL, no definite conclusion could be reached regarding the involvement of the studied mutations/polymorphisms in childhood AIS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_assertion evidence source_evidence_literature NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_assertion SIO_000772 16567932 NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_assertion wasDerivedFrom gad-20150221 NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_assertion wasGeneratedBy ECO_0000203 NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99675.RATc2fbfLSlp8H1JzrVAm8bf70VetsZCLfmeseeT9CqFw130_provenance.