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- source_evidence_literature type ECO_0000212 NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_assertion description "[Common polymorphisms of HF1 may contribute to D-HUS manifestation in subjects with and without HF1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_assertion evidence source_evidence_literature NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_assertion SIO_000772 14583443 NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_assertion wasDerivedFrom befree-20150227 NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_assertion wasGeneratedBy ECO_0000203 NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446559.RANm0fDHHhMmxRbJ7Apg37VEQ19_z5Nn1nn_VLjwflPSs130_provenance.